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Brilliant Technologies

Innovative Products

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CATALOGUECATALOGUEAn I l l u s t ra t i ve l i s t o f t he bes t

Six Sigma

Vol - I

Plant : # 338, Sector-2, Industrial Growth Centre, Saha-133104.Ph : 0171-3248775 - 76, Website : www.aveconhealthcare.com

E-mail : [email protected], [email protected]

Avecon Healthcare Pvt Ltd was incorporated in early March 2007 with the focused vision of applying advanced technologies for the development of world class products with unsurpassed quality.

Avecon truly recognizes the global need for innovative diagnostic products to be used in medical hospitals, pathological laboratories, nursing homes as well as for research and development purposes. Since inception, Avecon has been developing and manufacturing high-quality diagnostic products in the main manufacturing facility located in SAHA near the beautiful place Chandigarh (Union Territory of India).

Avecon Healthcare offers a full spectrum of pioneering diagnostic products ranging from Clinical Chemistry, Serology, Immuno Assay Kits (ELISAs') Rapid Tests, Coagulation and Immuno Turbidometry. Avecon's wide range of products includes Point Of Care Instruments for Diabetes assessment (Blood Glucose Monitoring System) and Biomedical Instruments like Semi/Fully automated analyzers for routine biochemistry and hematology investigations.

Avecon was formed by a group of professionals who are well known for their healthcare business since 19 years. The group represents more than 20 different Indian and Overseas companies and achieved the annual group turnover of 15 million USD

With the vision of becoming leading manufacturer in the chosen field Avecon has constructed a state of the art in-house manufacturing facility with sophisticated equipments to develop and manufacture latest generation products as per GMP, ISO and CE standards to meet the global requirements.

Avecon has already consolidated it's business modalities by outsourcing new product segments, establishing nation wide distributors net work and appointing trained field personnel to take care of all the major territories in India.

Avecon's technical team is continuously putting relentless efforts to expand company’s product portfolio and at the same time keeping the quality of its IVD products at the highest level by regular value additions and perfective maintenance. The main activities are in line with Avecon's core competence in the field of Clinical Chemistry and the company is now able to offer many of the ultra stable, ready to use clinical chemistry reagents that are capable of setting bench marks

Products that are manufactured at Avecon undergo stringent quality checks to meet the best standards in the industry.

As a value addition Avecon intends to incorporate Six Sigma methodologies to optimize and streamline the functions of all the departments in the organization.

The company has entered into strategic alliances with domestic / overseas medical diagnostic and device manufacturing companies to create an enviable portfolio with which the company shall become the trans-national operational site to transfer critical technologies and to cater it’s services globally.

In its quest to achieve the highest level of success Avecon aims at absolute customer satisfaction and prompt service. Avecon will continue to provide products and services that will enhance the customers’ medical care, health awareness and quality of life by assisting in the early diagnosis of different medical conditions in a cost effective manner.

Six Sigma ABOUT US

UNDERSTANDING SIX SIGMA :

Avecon incorporates Six Sigma concept to improve the overall efficiency of all the functional areas like Manufacturing, Administration, Customer Service, Research & Development, Quality Control, Purchase, Document Control, Sales/Marketing and Logistics. Six Sigma is a data driven management system with near perfect management objectives to improve the quality of organizational processes and was originally implemented in Motorola in 1980's for the first time. Six Sigma has become one of the most widely discussed and reported trends in business for the past two years and is now seen as a mandatory requirement in many organizations to yield tangible business results.

The Six Sigma concept has been developed into a methodology that focuses on process improvement and variation reduction through the use of a measurement - based strategy. This Six Sigma methodology is often accomplished through the use of DMAIC (Define, Measure, Analysis, Improve, and Control) as sub-methodology.

Six Sigma project team identifies quality requirements of an end product based on business objectives as well as customer needs and feedback. The team identifies CTQs (critical to quality characteristics) that are considered to have a maximum impact on quality. The team also identifies and separates “vital few” from “trivial many”.

The team identifies the key internal processes that influence CTQs and measures the defects currently generated.

The team discovers why defects are generated by identifying the key variables which are are most likely to create process variation.

The team identifies maximum acceptable ranges for the key variables and validates a system for measuring deviations of the variables. The team modifies the process in such a way that it stays within the acceptable

Tools are put in place to ensure that the key variables remain within the maximum acceptable ranges over time.

IMPROVE

CONTROL

MEASURE

ANALYZE

DEFINE

Six Sigma SIX SIGMA AND AVECON

SIX SIGMA, AVECON AND YOU.

A move towards Six Sigma is resulting in further improvements in our ways of thinking and ways of doing business, ultimately leading to quantum leaps in process and product quality in our main area of manufacturing. Our superior products are delivered in a timely manner and at the best possible price. This practice in turn translates into highly satisfied customers and increasing market place domination. The ultimate tangible results are Increased productivity, Reductions in recurring production costs, Reduced production cycle times and Reduced inventory levels.

Fig. : Schematic representation of Avecon’s Business Objectives

ON THE ROAD TO SIX SIGMA

Successful implementation of Six Sigma at Avecon is being achieved through careful planning & program control, benchmarking of all processes and the application of the roadmap. Rigorous controls, management of business models, designing products and processes are vital for Six Sigma. Six Sigma is implemented by achieving total management / employee support, instituting rigorous program controls and assuring proper training. The company has already started getting the fruits of its dedicated effort and relentless pursuance by implementing Six Sigma.

CustomerRequirements

MaterialCapabilities

ProcessCapabilities

RobustDesigns

SophisticatedInfrastructure

ConsistentPerformance

CustomerSatisafaction

TangibleBusiness Results

HighQuality

SuperiorReliability

On TimeDelivery

LowerCosts

Six Sigma SIX SIGMA AND AVECON

We shall become the customers’ “COMPANY OF CHOICE” in the field of In vitro Diagnostics through :

a) Adhering to all the National and International standards for producing high quality products using the latest innovative technologies.

b) Constant upgradation and the value addition of the products time to time.

c) Providing a conducive environment for the integrated functionaries and business associates.

d) Achieving excellence in all the fields through dedication, team work, commitment and conviction.

e) Incorporation of SIX SIGMA methodology DMAIC (Defining, Measuring, Analyzing, Improving & Controlling) throughout the manufacturing processes.

f) The Hallmarks of our products are Excellent performance, High reliability, Ease of use and Adaptability.

g) The Hallmarks of our service are On time delivery, Commitment to satisfy customer needs as and when required.

Researchand

Development

CUSTOMERNEEDS

TechnicalSupport

QualityAssurance

andQualityControl

Manufacturing

PackageDesign

andKit

Assembly

Distributionand

LogisticsSales,

Marketing,CustomerSupport

RegulatoryAffairs

Avecon’s Focus

Organizational Activities (A schematic diagram)

Six Sigma QUALITY POLICY

Six Sigma TABLE OF CONTENTS

IMMUNO TURBIDOMETRY A Premium and comprehensive TurbiMAX range of immuno turbidometry assay kits with PET (Particle Enhanced Technology)are made availble from Avecon to provide highest sensitivity and precision. These kits are available as ready to use liquid reagents specially designed for use on most of the semi and fully auto analyzer platforms. Single/ Multi level calibrator/calibrators provided along with the kits.

COAGULATIONLyophilized and Liquid stable coagulation reagents with highest precision are available for use manually and on coagulation analyzers. These reagents meet the guidelines of ICSH and ICHT to give the best performance. Batch specific ISI values are assigned.

RAPID TESTSHaving understood the requirements of Indian & Overseas customers, Instant View / MaxLINE / MaxView range of rapid tests for pregnancy and infectious diseases with Lateral flow immunochromatography test principle are made available from Avecon. These rapid tests are carefully designed to give highest level of performance in terms of sensitivity, specificity and reliability.

POINT OF CAREGood Point Of Care instruments should give quick and reliable results. Avecon has the ones’ with advanced biosensor technology which gives the results in just 5 seconds and the results correlate with manual laboratory cumbersome procedures.

INSTRUMENTATIONAvecon’s laboratory instruments are carefully selected as per the requirements of customers. They are equipped with latest technology, features and analytical precision. The range includes from simple colorimeters to advanced semi and fully auto analyzers. Have a look at the different analyzers for different applications.

MICRO PIPETTESA complete range of imported micro pipettes specially designed and crafted for fatigue free pipetting comfort are made available from Avecon to ensure highest level of precision, accuracy and reliability.

CLINICAL CHEMISTRYAvecon offers the complete LiquiMAX range of liquid stable reagents for End Point, Fixed Time and Kinetic Assays in Mono liquid and Bi liquid formats. These LiquiMAX reagents are designed for maximum stability, ease of use and are adaptable to most of the colorimeter and semi auto analyzer plat forms.

A premium AutoMAX product range of liquid stable reagents ( for End Point, Fixed Time and Kinetic Assays) are available in Mono liquid and Bi liquid formats from Avecon. These AutoMAX Reagents are designed and dedicated for use only on fully automated analyzers. AutoMAX reagents are available as individualized, dedicated and bar coded system packs especially

TMfor HITACHI 902 / 911/ 912/ 704 Analyzers.

SEROLOGYSeroMAX agglutination range of serology kits with PET (Particle Enhanced Technology) are the best choice for small and moderately big labs. These kits are designed to provide clear- cut agglutination for the samples that are in the cut off line. SeroMAX kits do not require sample dilution and neat serum can be tested.

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Clinical Chemistry

Ref./Cat. No. Pack Size

AVALB - 200 4 x 50 mlAVALB - 1000 2 x 500 ml

Salient Features :

1. Single Liquid Reagent.2. One step End Point assay.3. Superior over Methyl Orange and HABA dye methods4. Linearity : 10 gm/dl.5. Aqueous albumin standard provided6. Can be used on any colorimeter, spectrophotometer ,discrete semi automated and automated analyzers

LiquiMAX ALKALINE PHOSPHATASE - SLR IFCC/ AMP BUFFER / KINETIC


AVALP(SLR) - 25 25 x 1 ml

AVALP(SLR) - 50 50 x 1 ml

Salient Features :1. Single Liquid Reagent (Ready to use I No reconstitution required).2. Kinetic reaction time 2 minutes.

03. Kinetic factor 2757 at 405 nm at 37 C.4. Measuring wave length 405 nm.5. Linearity 1000 IU/L.6. Tailor made for Tropical conditions7. No interference is absorbed by triglycerides up to 2200mg/dI, bilimbun up to 42mg/dl

hemoglobin up to 150mg/dI, intra lipids up to 1200 mg/dI and ascorbic acid up to 32mg/dl

LiquiMAX ADA ENZYMATIC - FIXED TIME


AVADA (K) - 25 26 ml

AVADA (K) - 50 52 ml

(R1 : 2x9 ml, R2 : 2x4 ml)

(R1 : 4x9 ml, R2 : 4x4 ml)

Salient Features :1 . Two Liquid Reagents2. Kinetic Method. (5 Minutes First Incubation+ 5 Minutes Second Incubation)3. Linearity : 200 IU/L4. Kinetic reaction time 300 sec (60 Sec + 240 Sec.).5. Assay is not affected by Serum Bilirubin up to 20 mg/dL, Hemoglobin up to 200 mg/dL,

Triglycerides up to 750 mg/dL, and Ascorbic acid up to 4 mg/dL.6. Can be used on any discrete semi automated and automated analyzers.

Six Sigma

LiquiMAX ALBUMIN - SLR (BCG METHOD)

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Chemistry- End Point



AVADA (C) - 10 10 TestsAVADA (C) - 25 25 Tests

Salient Features :

1. Four Liquid Reagents 2. All the reagents are ready to use and there is no need for working reagent Preparations 3. Detects all the Iso enzymes of ADA (ADA 1m, ADA1c, ADA2)4. Two Step End Point Method.5. Linearity : 250 U/L6. Can be used on any colorimeter.

LiquiMAX ADA-MTBGlusti & Galanti Method

Chemistry- End Time


Chemistry- Kinetic


LiquiMAX ALKALINE PHOSPHATASE DEA BUFFER - DGKC METHOD

Ref./Cat. No. Pack SizeAVALP - 25 25 ml

AVALP - 50 50 ml

AVALP - 200 200 ml

(R1 : 5x4 ml, R2 : 5 ml)

(R1 : 5x8 ml, R2 : 10 ml)

(R1 : 20x8 ml, R2 : 4x10 ml)

Salient Features :1. Two Liquid Reagents (4 parts R1 + 1 part R2).2. working reagent stability of 1 month at 2-8 ºC.3. Auto hydrolysis prevented thereby good working reagent stability.4. Kinetic reaction time 2 minutes.5. Kinetic factor 2757 at 405 nm at 37° C.6. Linearity 1500 IU/L.7. Can be used on any discrete semi automated and automated analyzers8. No interference is absorbed by triglycerides up to 2200mg/dI, bilirubun up to 42mg/dl

hemoglobin up to 150mg/dI, intra lipids up to 1200 mg/dI and ascorbic acid up to 32mg/dl

Chemistry- Kinetic

Shelf Life - 18 Months5

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AVAMM (E) - 25 25 ml

AVAMM (E) -50 50 ml

(R1 : 5x4 ml, R2 : 5 ml)

(R1 : 10x4 ml, R2 : 10 ml)

Salient Features :

1. Two Liquid Reagents( 4 parts R1 + 1 part R2).

2. UV-Fixed Rate (Initial Rate) Method.

3. Linearity 600 µg/dl.

5. Working Reagent stability 7 days at 2-8°C.

7. C

4. Fixed reaction time 240 sec (60 Sec + 180 Sec.).

6. No significant interference was observed from Bilirubin up to 20 mg/dl (Both conjugated and

unconjugated Bilirubin), Lipernia as Triglycerides up to 2000 mg/dI, Ascorbic acid up to 30 mg/dI.

an be used on any discrete semi automated and automated analyzers

LiquiMAX AMYLASE - SLR CNPG METHOD3


AVAMY - 10 10 x 1 ml



Salient Features :1. Single Liquid Reagent. Available in mono test packs.

2. Uses CNPG3 as a Direct Chromogenic Substrate.

3. Achive s 98% hydrolysis.4. Reagent system does not require auxiliary enzymes like Galactosidase and Glucoamylase.5. One step kinetic assay. Kinetic reaction time 2 minutes.6. Linearity 2000 IU/L.7. Kinetic factor 3178 at 405 nm at 37° C.8. No interference from Bilirubin (up to 50 mg/dl), Ascorbate (up to 500 mg/dl), Glucose

(up to 5000 mg/dl).9. Can be used on any discrete semi automated a

Chemistry- Fixed Time


Chemistry- Kinetic


LiquiMAX BILIRUBIN - (DIRECT) (JENDRASSIK & GROF’S METHOD)


AVBIL (D) - 200 2 x 100 ml

AVBIL (D) - 1000 2 x 500 ml

Salient Features :

1. Two Liquid Reagents. 2. Neonatal bilirubin can be estimated. 3. 5 minutes End Point assay.4. Linearity 25 mg/dl.5. Can be used on any colorimeter, spectrophotometer ,discrete semi automated and automated analyzers.6. Incorporates Six Sigma methodologies throughout the manufacturing processes where in the

product under goes various stringent process checks like Defining, Measuring, Analyzing, Improving and Controlling. (DMAIC)



LiquiMAX BILIRUBIN - (TOTAL & DIRECT) (JENDRASSIK & GROF’S METHOD)


AVBIL (T&D) -180 6 x 30 ml

Salient Features :1. Separate Reagents for Total & Direct Bilirubin.2. Both Monochromatic and Bichromatic estimations.3. Neonatal bilirubin can be estimated.4. 5 minutes End Point assay.5. Linearity 25 mg/dl 6. Can be used on any colorimeter, spectrophotometer, discrete semi automated and automated

analyzers.7. Estmination with fixed factors : Total Bilirubin : 24 Direct Bilirubin : 13.5



LiquiMAX BILIRUBIN - (TOTAL) (JENDRASSIK & GROF’S METHOD)


AVBIL (T) - 200 2 x 100 ml

AVBIL (T) -1000 2 x 500 ml

Salient Features :1. Both Monochromatic and Bichromatic estimations.

6. Estmination with fixed factors : Total Bilirubin : 24

2. Neonatal bilirubin can be estimated. 3. 5 minutes End Point assay.4. Linearity 25 mg/dl.5. Can be used on any colorimeter, spectrophotometer, discrete semi automated and automated analyzers.



LiquiMAX CALCIUM (O - CPC METHOD)


AVCAL (O) -50 2 x 25 ml

AVCAL (O) -100 2 x 50 ml

AVCAL (O) -500 2 x 250 ml

(R1 : 25ml, R2 : 25ml)

(R1 : 50ml, R2 : 50ml)

(R1 : 250ml, R2 : 250ml)

Salient Features :

1. Two Liquid Reagents.2. Heating and centrifugation of specimen not required.3. Addition of 8-Hydroxy Quinolene overcomes Magnesium interference4. Results correlate with Arsenazo-III and Methyl Thymol Blue Methods.5. Linearity 25 mg/dl.6. Disposable calcium free test tubes provided for testing.9. No significant interference was observed from bilirubin up to 100 mg/dl, hemoglobin concentration up

to 200 mg/dl) Lipemia (Intralipid) as triglycerides concentration up to 1200 mg/dl.7. Can be used on any colorimeter, spectrophotometer ,discrete semi automated and automated

analyzers.

LiquiMAX CALCIUM - SLR (ARSENAZO III METHOD)


AVCAL (A) - 25 25 x 1 mlAVCAL (A) - 50 50 x 1 mlAVCAL (A) - 100 10 x 10 ml

Salient Features :1. Single Liquid Reagent. Available in mono test packs2. One step End Point assay3. Heating and centrifugation of specimen not required.4. Addition of 8-Hydroxy Quinolene overcomes Magnesium interference.5. Results correlate with (O-CPC) and Methyl Thymol Blue Methods.6. Linearity 25 mg/dl.7. No significant interference was observed from Bilirubin up to 20 mg/dl (Both conjugated and

unconjugated Bilirubin) Hemoglobin up to 50 mg/dl,Lipemia as Triglycerides up to 2000 mg/dl, Ascorbic acid up to 50 mg/dl.

8. Can be used on any colorimeter, spectrophotometer, discrete semi automated and automated analyzers.

LiquiMAX CHLORIDE - SLR (MTC METHOD)


AVCHL - 50 2 x 25 ml

AVCHL - 100 2 x 50 ml

Salient Features :

1. Single Liquid Reagent.2. One step End Point assay.3. Results correlate with ISE , Direct and Indirect potentiometry.4. No pretreatment of the sample required.5. Linearity:150 mMol/L6. Can be used on any colorimeter, spectrophotometer, discrete semi automated and automated analyzers

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LiquiMAX CHOLESTEROL-SLR (CHOD/PAP TRINDER’S METHOD)


AVCHO(5) - 50 2 x 25 ml

AVCHO(5) - 100 4 x 25 ml

AVCHO(5) - 250 5 x 50 ml

AVCHO(5) - 500 10 x 50 ml

Salient Features :

1. Single Liquid Reagent.2. 5 minutes End Point assay3. Linearity: Total Cholesterol 1000 mg/dl. 4. With Lipid Clearing Factor (LCF).5. No significant interference was observed from bilirubin up to 20 mg/dl, hemoglobin up to 450 mg/dl)

and triglycerides 1250 mg/dl.6. Can be used on any colorimeter, spectrophotometer, discrete semi automated and automated

analyzers

LiquiMAX CHOLESTEROL-Instamix(CHOD/PAP TRINDER’S METHOD)


AVCHO(2) - 50 2 x 25 ml

AVCHO(2) - 100 4 x 25 ml

AVCHO(2) - 250 5 x 50 ml

AVCHO(2) - 500 10 x 50 ml

Salient Features :

1. Two Liquid Reagent.2. 5 minutes End Point assay, 12 months working reagent stability3. Linearity: Total Cholesterol 1000 mg/dl. 4. With Lipid Clearing Factor (LCF).5. No significant interference was observed from bilirubin up to 20 mg/dl, hemoglobin up to 450 mg/dl)

and triglycerides 1250 mg/dl.6. Can be used on any colorimeter, spectrophotometer, discrete semi automated and automated

analyzers




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LiquiMAX CHOLINESTERASE KINETIC/ PHOTOMETRIC METHOD


AVCHE (E) 10 10 ml

(R1 : 5 ml, R2 : 5 ml, R3 : .4 ml)

Salient Features :1. Three Liquid Reagents (R1,R2, R3).2. Measuring wavelength 405 nm.3. Linearity 8000 U/L.4 Kinetic reaction time 2 minutes5. Kinetic factor 7820 at 405 nm at 37° C.6. No significant interference up to approximate bilirubin concentration : 45 mg/dl, hemoglobin

concentration : 1000 mg/dl, triglycerides concentration : 1500mg/dl7. Can be used on any discrete semi automated and automated analyzers.

Chemistry- Kinetic


LiquiMAX CK - MB (NAC ACT) MODIFIED IFCC METHOD

Ref./Cat. No. Pack Size AVCMB - 10 10 ml

AVCMB - 20 20 ml

AVCMB - 50 50 ml

(R1 : 1x8 ml, R2 : 1x2 ml)

(R1 : 2x8 ml, R2 : 2x2 ml)

(R1 : 2x20 ml, R2 : 2x5 ml)

Salient Features :1. Two Liquid Reagents (4 parts R1+ 1 part R2).2. Working reagent stability 10 days at 2-8° C.3. Linearity 1000 U/ML.4. Kinetic reaction time 10 minutes.5. Kinetic factor 6666 at 340 nm at 37° C.6. Measuring wavelength 340 nm.7. Can be used on any discrete semi automated and automated analyzers

LiquiMAX CK - NAC (NAC ACT)MODIFIED IFCC METHOD


AVNAC - 10 10 ml

AVCMB - 20 20 ml

AVCMB - 50 50 ml

(R1 : 1x8 ml, R2 : 1x2 ml)

(R1 : 2x8 ml, R2 : 2x2 ml)

(R1 : 2x20 ml, R2 : 2x5 ml)

Salient Features :1. Two Liquid Reagents (4 parts R1+1 part R2)2. Working reagent stabilty 10 days at 2-8° C.3. Linearity 2000 IU/L.4. Kinetic reaction time 5 minutes.5. Kinetic factor 8095 at 340 nms at 37 degrees.6. Measuring wavelength 340 nm.7. Can be used on any discrete semi automated and automated analyzers

LiquiMAX CREATININE- END POINT & FIXED TIME (MODIFIED JAFFE’S METHOD)


AVCRE(CE) 100 2 x 50 ml

AVCRE(CE) 200 2 x 100 ml

Salient Features :1. Both End Point & Fixed Time procedures.2. Three Liquid Reagents for End Point. (10 minutes End Point assay).3. Two Liquid Reagents for Fixed Time.(2 minutes Fixed Time assay)4. Working Reagent stability- 15 days at Room Temperature.5. With Lipid Clearing Factor (LCF).6. Linearity 25 mg/dl.7. C8. No significant interference was observed from Bilirubin up to 20 mg/dl (Both conjugated and


an be used only on colorimeter & Semi Auto Analyzers.

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LiquiMAX CREATININE - SLR MODIFIED JAFFE’S METHOD


AVCRE (SR) -100 4 x 25 ml

AVCRE (SR) - 300 6 x 50 ml

AVCRE (SR) - 500 10 x 50 ml

Salient Features :1. Single Liquid Reagent.2. Fixed Time / Initial Rate / Two Point Kinetic Method.3. 2 minutes fixed time assay (30 sec+90 sec).4. Linearity 25 mg/dl.5. With Lipid Clearing Factor (LCF).6. No significant interference was observed from Bilirubin up to 20 mg/dl (Both

conjugated and unconjugated Bilirubin) Hemoglobin up to 50 mg/dl,Lipemia as Triglycerides up to 2000 mg/dl, Ascorbic acid up to 50 mg/dl.

7. Can be used on any discrete semi automated and automated analyzers.

Chemistry-


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LiquiMAX ETHNOL-UV ( ENZYMATIC)


AVETL (E) - 25 5 x 5 ml

AVETL (E) - 50 10 x 5 ml

Salient Features :

1. World’s fastest Single Liquid Reagent.2. 3 minutes End Point assay 3. Linearity: Total Cholesterol 1000 mg/dl.4. With Lipid Clearing Factor (LCF).5. Can be used on any colorimeter, spectrophotometer, discrete semi automated and automated analyzers



Plz check No. 20

LiquiMAX G6PDH (QUANTITATIVE / KINETIC) ENZYMATIC/ UV METHOD


AVG6P(QT) - 10 10 ml

AVG6P(QT) - 20 20 ml

Salient Features :

1. Three Liquid Reagents with optional Lysing Reagent.

2. G6P-DH activity in serum, plasma and erythrocytes can be estimated.

3. Quantitative estimation.

4. Measuring wavelength 340 nm.

5. Can be used on any discrete semi automated and automated analyzers

LiquiMAX G6P-DH (QUALITATIVE / VISUAL)


AVG6P(QL)-12 12 Tests

Salient Features :

1. Qualitative visual dye decolourization method .2. Reagents ensuring complete inhibition of 6-Phophogluconate Dehydrogenase, thereby

giving better accuracy.3. Very convenient pack sizes.4. Giving additional reagent for running a control in dye decolourization.5. Q.A. procedures to ensure very high quality, high precision.6. Complete inhibition of 6-Phosphogluconate Dehydrogenase.7. Lysing reagent provided for the lysis of RBC. Visual interpretation of results8. One free test is available for running control sample9. Blood sample designed as per Hb concentration10. No instrumentation required.

LiquiMAX GLUCOSE InstaMIX- SLR (GOD - POD METHOD)


AVGLU (1) - 500 500 ml

AVGLU - 500 500 ml

AVGLU(I) - 1000 4 x 250 ml

(R1 : 2x237.5 ml, R2 : 2x12.5 ml)

(R1 : 4x118.75 ml, R2 : 4x6.25 ml)

(R1 : 4x337.50 ml, R2 : 4x12.5 ml)

Salient Features :1. 10 minutes End Point assay.2. Linearity: 500 mg/dl (End Point), 1000mg/dl (Fixed Time)3. With Lipid Clearing Factor (LCF) 4. 100 mg/dl & 300 mg/dl standards provided.5. Fixed Time & End Point procedures.6. Can be used on any colorimeter, spectrophotometer, discrete semi automated and automated analyzers

LiquiMAX GLUCOSE - SLR (GOD - POD METHOD)


AVGLU (1) - 500 5 x 100 ml

AVGLU - 500 2 x 250 ml

AVGLU - 500 5 x 100 ml

AVGLU(I) - 1000 4 x 250 ml

Salient Features :

1. Single Liquid Reagent.

2. 10 minutes End Point assay.3. Linearity: 500 mg/dl (End Point), 1000mg/dl (Fixed Time)4. With Lipid Clearing Factor (LCF) 5. 100 mg/dl & 300 mg/dl standards provided.6. Fixed Time & End Point procedures.7. Can be used on any colorimeter, spectrophotometer, discrete semi automated and automated analyzers

LiquiMAX GAMMA - GT (OPTIMIZED)IFCC METHOD

Ref./Cat. No. Pack SizeAVGGT - 15 15 x 1 ml

Salient Features :1. Uses Glupa-C as substrate(L-g-glutaryl-3-carboxy-4-nitroanilide).2. Linearity 300 IU/L.3. Measuring wavelength 405 nm.4. Kinetic reaction time 2 minutes.5. Kinetic factor 1158 at 405 nm at 37 degrees 7. C8. No significant interference was observed from Bilirubin up to 20 mg/dI (Both conjugated and

unconjugated Bilirubin) Hemoglobin up to 50 mg/dl,Lipemia as Triglycerides up to 2000 mg/dI, Ascorbic acid up to 50 mg/dI.

an be used on any discrete semi automated and automated analyzers.


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LiquiMAX GLYCOSYLATED HEMOGLOBIN (ION EXCHANGE RESIN METHOD)


AVGHB (A1) - 10 10 Tests

AVGHB (A1) - 20 20 Tests

Salient Features :

1. Weak cation exchange resin method.2. Selectively isolates GHB from Non GHB.3. Borate buffer removes 80% of labile fraction of GHB.4. Aldimine elimination prevents falsely elevated results.5. Results by factor6. Measuring wavelength 415 nm7. MBG and HB A1C can be reported from the formula8. Calibrator not required9. Can be used on any colorimeter, discrete semi automated analyzers

LiquiMAX HDL CHOLESTEROL (PHOSPHOTUNGSTATE METHOD)

Ref./Cat. No. Pack SizeAVHDL(P) - 50 2 x 25 mlAVHDL(P) - 100 2 x 50 ml

Salient Features :

1. To be used with Cholesterol-SLR Kits.2. HDL cholesterol standard provided.3. Linearity 150 mg/dl.4. Precipitation of serum sample required.5. Can be used on any colorimeter, spectrophotometer, discrete semi automated and automated analyzers

LiquiMAX HDL CHOLESTEROL -DIRECT (HOMOGENOUS/DETERGENT SELECTION METHOD)


AVHDL(DL)-40 40 ml

AVHDL(DL)-80 80 ml

AVHDL(DL)-160 160 ml

AVHDL(DL)-320 320 ml

(R1 : 1 x 30 ml, R2 : 1 x 10 ml)

(R1 : 2 x 30 ml, R2 : 2 x 10 ml)

(R1 : 2 x 60 ml, R2 : 2 x 40 ml)

(R1 : 4 x 60 ml, R2 : 2 x 40 ml)

Salient Features :

1. Two Liquid Reagents with Calibrator.2 End Point/Fixed Time procedures can be performed.3. Linearity range 3.7-200 mg/dl.4. No offline pre treatment of serum samples required5. Results correlate with other reference methods. 6. Meets NCEP guidelines.7. Works well with fasting & non fasting patient samples.8. Precision with high triglyceride samples.9. Can be used on any spectrophotometer, discrete semi automated and automated analyzers.

LiquiMAX MaxClean WASH SOLUTION


AVCWS-200 4 x 50 ml

LiquiMAX HEMOGLOBIN A1C (MICRO COLUMN METHOD)


AVHGB (A1C) - 20 20 Tests

Salient Features :

1. Micro column chromatography.2. Results by factor3. Measuring wavelength 415 nm4. Good accuracy and precision (CV below 5%)5. Temperature independent6. Results can be converted in to IFCC and NGSP methods.7. MBG can be calculated.8. Can be used on any colorimeter, discrete semi automated analyzers

LiquiMAX IRON/TIBC (FERROZINE/PHOTOMETRIC METHOD)


AVITB - 20 10 + 10 Tests

AVITB - 40 20 + 20 Tests

Salient Features :

1. Three Liquid Reagents. 2 Heating & Centrifugation of sample not required.3. Deproteinization of sample not required.4. Linearity: IRON 500 µg/dl, UIBC 500 µg/dl.5. Superior over Thio-cyanate, O-Phenanthroline, Bathophenanthroline & TPTZ.6. With Lipid Clearing Factor (LCF).7. C

8. Overcomes critical limitations of Friedewald formula.9. Works well with fasting & non fasting patient samples.

an be used on any colorimeter, spectrophotometer ,discrete semi automated and automated analyzers


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Salient Features :

1. Liquid Single Reagent2. Flow ced & Cuvette Cleaning Solutions.

LiquiMAX LDL CHOLESTEROL- DIRECT (HOMOGENOUS/DETERGENT SELECTION METHOD)


AVLDL(DL)-40 40 ml

AVLDL(DL)-80 80 ml

AVLDL(DL)-160 160 ml

AVLDL(DL)-320 320 ml

(R1 : 1 x 30 ml, R2 : 1 x 10 ml)

(R1 : 2 x 30 ml, R2 : 1 x 20 ml)

(R1 : 2 x 60 ml, R2 : 2 x 20 ml)

(R1 : 4 x 60 ml, R2 : 4 x 20 ml)

Salient Features :1. Two Liquid Reagents with Calibrator. End Point/Fixed Time procedures can be performed.2. Linearity range : 6.6 - 450 mg/dl (Semi Auto Analyzer Systems)

3.7 - 1000 mg/dl (Fully Auto Analyzer Systems)3. No offline pre treatment of serum samples required. Meets NCEP guidelines.5. Correlation with gold standard Beta quantification & Immuno separation.6. Overcomes critical limitations of Friedewald formula.7. Works well with fasting & non fasting patient samples.8. Precision with high triglyceride samples upto 1500 mg /dL9. C10. No significant interference was observed from Bilirubin up to 30 mg/dl (Both conjugated and


an be used on any spectrophotometer, discrete semi automated and automated analyzers

LiquiMAX LIPASE ENZYMATIC - COLORIMETRIC METHOD


AVLIP - 12 12 ml

AVLIP - 50 50 ml

(R1 : 1 x 10 ml, R2 : 1 x 2 ml)

(R1 : 2 x 21 ml, R2 : 2 x 4 ml)

Salient Features :

1. Two Liquid Reagents.2. Uses 1,2-O-dilauryl-rac-glycero-3glutaric acid (6’-menthlresorufin)-ester as

Lipase Specific Substrate.3. Measuring wavelength 578 nm. and Kinetic reaction time 3 min.4. Kinetic factor 1150 at 37 degree.5. Linearity 180 U/L.6. Can be used on any discrete semi automated and automated analyzers.

LiquiMAX LDH (L--- P)> IFCC METHOD


AVLDH - 10 10 ml

AVLDP - 20 20 ml

(R1 : 1 x 8 ml, R2 : 1 x 2 ml)

(R1 : 2 x 8 ml, R2 : 2 x 2 ml)

Salient Features :1. Two Liquid Reagents(4 parts R1+ 1 part R2).2. Lactate --- Pyruvate.>3. Linearity 1500 IU/L.4. Measuring wavelength 340 nm.5. Kinetic reaction time 4 minutes.6. Kinetic factor 8095 at 340 nm at 37 degrees 7. C8. No interference was observed by ascorbic acid up to 30 mg/di, billinubin up to 40 mg/dI and

lipemia up to 2,000 mg/dI triglycerides. Hemoglobin interferes starting with a concentration of 50 mg/dI.


LiquiMAX LACTATEENZYMATIC


AVLAC(E) - 25 5 x 5 ml

AVLAC(E) - 50 10 x 5 ml

Salient Features :1. Two Liquid Reagents(4 parts R1+ 1 part R2).2.

LiquiMAX LDH — P IFCC METHOD/ UV KINETIC


AVLDP - 10 10 ml

AVLDP - 20 20 ml

(R1 : 1 x 8 ml, R2 : 1 x 2 ml)

(R1 : 2 x 8 ml, R2 : 2 x 2 ml)

Salient Features :1. Two Liquid Reagents(4 parts R1+ 1 part R2).2. Pyruvate --- Lactate.>3. Linearity 2000 IU/L.4. Measuring wavelength 340 nm.5. Kinetic reaction time 4 minutes.6. Kinetic factor 8095 at 340 nm at 37 degrees 7. C8. No interference was observed by ascorbic acid up to 30 mg/di, billinubin up to 40 mg/dI

and lipemia up to 2,000 mg/dI triglycerides. Hemoglobin interferes starting with a concentration of 50 mg/dI.



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LiquiMAX PHOSPHORUS - SLR MOLYBDATE - UV METHOD


AVPHO - 100 4 X 25 ml

Salient Features :

1. Single Liquid Reagent.2. 5 minutes End Point assay.3. Linearity 20 mg/dl.4. No deproteinization of the sample required5. Superior over Phenyl hydrazine and Amino naphtho sulphonic acid methods6. With Lipid Clearing Factor (LCF).7 Can be used on any colorimeter, spectrophotometer, discrete semi automated and automated analyzers.8. No Significant interference was observed from bilirubin up to 92 mg/dl, hemoglobin up to 1100

mg/dl, and triglycerides up to 1650 mg/dl

LiquiMAX POTASSIUM (K+) - SLR (OPTIMIZED) (COLORIMETRIC METHOD)


AVPOT- 50 50 Tests

AVPOT- 100 100 Tests

AVPOT- 200 200 Tests

Salient Features :

1. Single Liquid Reagent.2. Linearity : 7 mMol/L.3. 5 minutes End Point assay4. Results corelate with ISE, Direct / Indirect potentiometry & flame photometry.5. Can be used on any colorimeter,spectrophotometer, discrete semi automated and automated analyzers6. No interference was observed by ascorbic acid up to 32 mg/dl, bilirubin up to 43 mg/dl, lipemia

up to 2200 mg/dl

LiquiMAX SGOT (AST) IFCC METHOD

Ref./Cat. No. Pack SizeAVGOT (E) - 50 50 ml

AVGOT (E) - 100 100 ml

AVGOT (E) - 250 250 ml

AVGOT (E) - 500 500 ml

(R1 : 5 x 8 ml, R2 : 1 x 10 ml)

(R1 : 4 x 20 ml, R2 : 1 x 20 ml)

(R1 : 5 x 50 ml, R2 : 1 x 50 ml)

(R1 : 8 x 50 ml, R2 : 2 x 50 ml)

Salient Features :1. Two Liquid Reagents (4 parts of R1 + 1 part of R2).2. Working reagent stability of 2 months at 2-8° C.3. Linearity 500 IU/L.4. Kinetic reaction time 4 minutes.5. Kinetic factor 1746 at 340 nm at 37° C.6. Measuring wavelength 340 nm.7. Can be used on any discrete semi automated and automated analyzers.8. No interference was observed by ascorbic acid up to 32 mg/dl, bilirubin up to 43 mg/dl,

hemoglobin up to 500 mg/dl and lipemia up to 2200 mg/dl triglycerides.


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ELiquiMAX MAGNESIUM - SLR (OPTIMIZED) (XYLIDYL BLUE/COLORIMETRIC METHOD)


AVMAG - 25 25 x 1 ml

AVMAG - 50 2 x 25 ml

Salient Features :

1. Single Liquid Reagent. Available in mono test packs.2. Overcomes calcium, heavy metals and protein interferences.3. Results correlate with atomic absorption.4. Linearity 5 mg/dl.5. 10 minutes End Point assay.6. With Lipid Clearing Factor (LCF)7. Can be used on any colorimeter, spectrophotometer, discrete semi automated and automated

analyzers.

8. No significant interference was observed from Bilirubin up to 10 mg/dl and Intralipid as

triglycerides up to 950 mg/dl

LiquiMAX MICROPROTEIN - SLR (PYROGALLOL RED METHOD)


AVMPR - 50 2 x 25 ml

AVMPR - 100 4 x 25 ml

Salient Features :

1. Single Liquid Reagent.2. Linearity 250 mg/dl.3. Superior over sulphosalicylic acid method.4. 5 minutes End Point assay.5. Results correlate with Benzethonium Chloride method.6. Detects Microprotein as low as 4 mg/dl.7. Can be used on any colorimeter, spectrophotometer, discrete semi automated and automated

analyzers.8. No significant interference was observed from conjugated and unconjugated bilirubin

concentration up to 20 mg/dl, haemoglobin up to 50 mg/dl, Ascorbic Acid, Creatinine, Glucose Phosphorus, Urea, Magnesium, Sodium Citrate, Caffeine, Cefazolin Sodium, Chlorpromazine Calcium, L-Dopa, Gentamicin Sulfate, Sodium Oxalate and Uric Acid.





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LiquiMAX SODIUM (Na+) POTASSIUM (K+) (OPTIMIZED) COLORIMETRIC METHOD


AVNAK - 60 30 + 30 Tests

Salient Features :1. Single Liquid Reagent for Potassium Estimation.2. Two Liquid Reagents for Sodium Estimation.3. Linearity Sodium : 200 mMol/L, Potassium : 7 mMol/L4. Results corelate with ISE, Direct/ Indirect Potentiometry & Flame Photometry.5. C

6.

an be used on any colorimeter, spectrophotometer, discrete semi automated analyzers

No interference was observed by ascorbic acid up to 32 mg/dl, bilirubin up to 43 mg/dl, hemoglobin up to 500 mg/dl and lipemia up to 2200 mg/dl triglycerides.

LiquiMAX SODIUM (Na+) (OPTIMIZED) COLORIMETRIC METHOD


AVNA - 100 100 Tests

Salient Features :1. Two Liquid Reagents for Sodium Estimation.2. Linearity Sodium : 200 mMol/L, 3. Results corelate with ISE, Direct/ Indirect Potentiometry & Flame Photometry.4. Tailor made for Tropical Conditions.5. Can be used on any colorimeter, spectrophotometer, discrete semi automated analyzers6. No interference was observed by ascorbic acid up to 32 mg/dl, bilirubin up to 43 mg/dl,


LiquiMAX TOTAL PROTEIN - SLR BIURET METHOD


AVTPN - 200 4 x 50 ml

Salient Features :

1. Single Liquid Reagent.2. 5 minutes End Point assay.3. With Lipid Clearing Factor (LCF).4. Linearity Total Protein : 10 gm/dl.5. Aqueous protein standard provided.6. Can be used on any colorimeter,spectrophotometer, discrete semi automated and automated analyzers

LiquiMAX SGPT (ALT) IFCC METHOD

Ref./Cat. No. Pack SizeAVGPT (E) - 50 50 ml

AVGPT (E) - 100 100 ml

AVGPT (E) - 250 250 ml

AVGPT (E) - 500 500 ml

(R1 : 5 x 8 ml, R2 : 1 x 10 ml)

(R1 : 4 x 20 ml, R2 : 1 x 20 ml)

(R1 : 4 x 50 ml, R2 : 1 x 50 ml)

(R1 : 8 x 50 ml, R2 : 2 x 50 ml)

Salient Features :1. Two Liquid Reagents (4 parts of R1 + 1 part of R2).2. Working reagent stability of 2 months at 2-8° C.3. Linearity 500 IU/L.4. Kinetic reaction time 4 minutes.5. Kinetic factor 1746 at 340 nm at 37° C.6. Measuring wavelength 340 nm.7 C8.

an be used on any discrete semi automated and automated analyzers.No interference was observed by ascorbic acid up to 32 mg/dl, bilirubin up to 43 mg/dl, hemoglobin up to 500 mg/dl and lipemia up to 2200 mg/dl triglycerides.


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ELiquiMAX SGOT (AST) ( REITMAN & FRANKEL’S COLORIMETRIC DNPH METHOD)


AVGOT(C) - 30 30 Tests

Salient Features :

1. Three Liquid Reagents.2. Avoids cumbersome graph preparation. No need to plot any standard curve.3. No inhibitory intermediate products produced during the assay.4. Results correlate with UV-Kinetic Method.5. Calibrator is calibrated against WHO AST (E.C.2.6.1.1) enzyme calibrator.6. For colorimeters only.7. No interference was observed by ascorbic acid up to 32 mg/dl, bilirubin up to 43 mg/dl,


LiquiMAX SGPT (ALT) (REITMAN & FRANKEL’S COLORIMETRIC DNPH METHOD)


AVGPT (C) - 30 30 Tests

Salient Features :

1. Three Liquid Reagents.2. Avoids cumbersome graph preparation. No need to plot any standard curve.3. No inhibitory intermediate products produced during the assay.4. Results correlate with UV-Kinetic Method.5. Calibrator is calibrated against WHO AST (E.C.2.6.1.2) enzyme calibrator.6. For colorimeters only.7. No interference was observed by ascorbic acid up to 32 mg/dl, bilirubin up to 43 mg/dl, hemoglobin up

to 500 mg/dl and lipemia up to 2200 mg/dl triglycerides.





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LiquiMAX URIC ACID - SLR (AOX/TOOS) URICASE - PAP TRINDER’S METHOD


AVURI (2) - 25 25 ml

AVURI (2) - 50 2 x 25 ml

AVURI (2) - 100 4 x 25 ml

AVURI (2) - 250 5 x 50 ml

AVURI (2) - 500 10 x 50 ml

Salient Features :1. Single Liquid Reagent.2. Linearity 30 mg/dl.3. Incorporates Ascorbate Oxidase to overcome Ascorbic acid interference.4. With *TOOS as Chromogen (*N-ethyl-N-(2-hydroxy-3-sulphopropyl)-m-toluidine).5. With Lipid Clearing Factor (LCF).6. 5 Minutes End Point Assay.7. Can be used on any spectrophotometer, discrete semi automated and automated analyzers.8. No significant interference was observed from bilirubin up to 20 mg/dl(Both conjugated &

unconjugated Bilirubin) hemoglobin up to 50 mg/dl and lipemia up to 2000 mg/dl triglycerides,Ascorbic acid up to 30 mg/dl

LiquiMAX URIC ACID - SLR (TBHBA) URICASE - PAP TRINDER’S METHOD


AVURI (1) - 25 25 ml

AVURI (1) - 50 2 x 25 ml

AVURI (1) - 100 4 x 25 ml

AVURI (1) - 250 5 x 50 ml

AVURI (1) -500 10 x 50 ml

Salient Features :1. Single Liquid Reagent.2. Linearity 30 mg/dl.3. With *TBHBA as Chromogen. (*TBHBA = 2,4,6 Tribromo 3 Hydroxy Benzoic Acid).4. With Lipid Clearing Factor (LCF).5. 10 Minutes End Point Assay.

6. Can be used on any colorimeter, spectrophotometer, discrete semi automated and automated analyzers.7. No significant interference was observed from bilirubin up to 20 mg/dl(Both conjugated &


LiquiMAX UREA - GLDH UREASE - GLDH METHOD


AVURE (E) -100 100 ml

AVURE (E) - 250 250 ml

AVURE (E) - 500 500 ml

(R1 : 4x20 ml, R2 : 20 ml)

(R1 : 4x50 ml, R2 : 1x50 ml)

(R1 : 8x50 ml, R2 : 4 x 50 ml)

Salient Features :1. Two Liquid Reagents( 4 parts R1 + 1 part R2).2. UV-Fixed Rate (Initial Rate) Method.3. Linearity 350 mg/dl.4. Fixed reaction time 90 sec (30+60).5. BUN values can be estimated.6. Working reagent stability of 2 months at 2-8°C.7. Can be used on any discrete semi automated and automated analyzers. 8. No significant interference was observed from bilirubin up to 20 mg/dl(Both conjugated &


LiquiMAX UREA MODIFIED BERTHELOT METHOD


AVURE (B) - 50 (Det) 2 x 50 ml

AVURE (B) -100(Det) 2 x 100 ml

AVURE (B) -200(Det) 4 x 100 ml

AVURE(B)- 500 (Det) 2 x 500 ml

(R1 : 50ml, R2 : 50ml)

(R1 : 100ml, R2 : 100ml)

(R1 : 2x100ml, R2 : 2x100ml)

(R1 : 5x100ml, R2 : 5x100ml)

Salient Features :1. Two Liquid Reagents with Enzyme concentrate2. Working Reagent Stability- 12 months at 2-8°C.3. With Lipid Clearing Factor (LCF).4. 8 Minutes two step End Point assay.5. Linearity - 350 mg/dl.6. BUN values can be estimated.7 Can be used on any colorimeter, spectrophotometer, discrete semi automated and automated

analyzers.8. No interference was observed by ascorbic acid up to 32 mg/dl, bilirubin up to 43 mg/dl,



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ELiquiMAX TRIGLYCERIDES - SLR (TBHBA) GPO - PAP TRINDER’S METHOD


AVTGL(1) - 25 25 mlAVTGL(1) - 50 2 x 25 mlAVTGL(1) - 100 4 x 25 mlAVTGL(1) - 250 5 x 50 mlAVTGL(1) - 500 10 x 50ml

Salient Features :1. Single Liquid Reagent.2. Linearity 1200 mg/dl.3. With*TBHBA as Chromogen (*2,4,6-Tribromo-3-hydroxy-benzoic acid).4. 10 Minutes End Point Assay.5. Excellent correlation with INT & UV methodologies6 Can be used on any colorimeter, spectrophotometer, discrete semi automated and automated

analyzers7. No interference was observed by ascorbic acid up to 32 mg/dl, bilirubin up to 43 mg/dl,






Chemistry-


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E AutoMAX ALBUMIN BCG METHOD


AVALB (A) - 200 4 x 50 ml

AVALB (A) - 400 8 x 50 ml

Salient Features :

1. Individualized, Dedicated, Bar coded System Packs forHitachi 902/911/912/704 Analyzers & other open systems.

2. Single Liquid Reagent.3. One step End Point assay.4. Superior over Methyl Orange and HABA dye methods5. Linearity : 10 gm/dl.6. Aqueous albumin calibrator provided.7. Programme sheets available for different analyzers.

AutoMAX ALKALINE PHOSPHATASE DEA BUFFER / DGKC METHOD


AVALP (A) - 200 200 ml

(R1 : 4 x 40 ml, R2 : 2 x 20 ml)

Salient Features :


2. Two Liquid Reagents (4 parts R1 + 1 part R2).3. Auto hydrolysis prevented thereby good onboard stability.4. Results by calibration with commercial calibrators OR by Kinetic factor 2757 at

405 nm at 37° C.5. Linearity 1500 IU/L.6. Measuring wave length 405 nm.7. Programme sheets available for different analyzers.

AutoMAX AMYLASE CNPG3 METHOD


AVAMY (A) - 100 5 x 20 ml

Salient Features :


2. Single Liquid Reagent.3. Uses CNPG3 as a Direct Chromogenic Substrate.4. Achives 98% hydrolysis in a single step .5. Linearity 2000 IU/L.6. Measuring wavelength 405 nm.7. Results by calibration with commercial calibrators OR by Kinetic factor 3178 at

405 nm at 37° C.8. Programme sheets available for different analyzers.

AutoMAX BILIRUBIN- (DIRECT) JENDRASSIK & GROF’S METHOD


AVABILT (A) - 200 4 x 50 ml


Salient Features :

1. Indivi

Six Sigma Clinical Chemistry

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AutoMAX CHOLESTEROL CHOD-PAP TRINDER’S METHOD


AVCHO (A) - 200 4 x 50 ml

AVCHO (A) - 400 8 x 50 ml

AVCHO (A) - 800 16 x 50 ml

Salient Features :


2. Single Liquid Reagent.3. Linearity: Total Cholesterol 1000 mg/dl4. With Lipid Clearing Factor (LCF).5. Aqueous calibrator provided.6. Programme sheets available for different analyzers.

AutoMAX CK - MB IFCC METHOD


AVCMB (A) -100 2 x 50 ml

AVCMB (A) -200 4 x 50 ml

(R1 : 2x40ml, R2 : 10ml)

(R1 : 4x40ml, R2 : 4x10ml)

Salient Features :


2. Two Liquid Reagents (4 parts R1+ 1 part R2).3. Linearity 2000 IU/L.4. Measuring wavelength 340 nm.5. Results by calibration with commercial calibrators OR by Kinetic factor 1651 at 340 nm at 37° C.6. Programme sheets available for different analyzers.


AutoMAX CALCIUM ARSENAZO III ARSENAZO III METHOD


AVCAL (AA) - 200 4 x 50 ml

AVCAL (AA) - 400 8 x 50 ml

Salient Features :


2. Single Liquid Reagent.3. One step End Point assay4. Heating and centrifugation of specimen not required. 5. Addition of 8-Hydroxy Quinolene overcomes Magnesium interference.6. Results correlate with (O-CPC) and Methyl Thymol Blue Methods.7. Linearity 25 mg/dl.8. Aqueous calibrator provided.9. Programme sheets available for different analyzers.

AutoMAX BILIRUBIN- (TOTAL) JENDRASSIK & GROF’S METHOD




Salient Features :

1. Individualized, Dedicated, Bar coded System Packs forHitach.

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AutoMAX GAMMA - GT SZASZ METHOD


AVGGT (A) - 100 100ml

(R1 : 2x40ml, R2 :2 x 10ml)

Salient Features :


2. Two Liquid Reagents(4 parts R1+ 1part R2).3. Uses Glupa-C as substrate(L-g-glutaryl-3-carboxy-4-nitroanilide).4. Linearity 350 IU/L.5. Measuring wavelength 405 nm.6. Results by calibration with commercial calibrators OR by Kinetic factor 1158 at 405 nm at 37° C.7. Programme sheets available for different analyzers.

AutoMAX CHLORIDE MTC METHOD


AVGGT (A) - 100 2 x 50ml

(R1 : 2x40ml, R2 :20ml)

Salient Features :

1. I

nt analyzers.

ndividualized, Dedicated, Bar coded System Packs forHitachi 902/911/912/704 Analyzers & other open systems.

2. Two Liquid Reagents(4 parts R1+ 1part R2).3. Uses Glupa-C as substrate(L-g-glutaryl-3-carboxy-4-nitroanilide).4. Linearity 350 IU/L.5. Measuring wavelength 405 nm.6. Results by calibration with commercial calibrators OR by Kinetic factor 1158 at 405 nm at 37° C.7. Programme sheets available for differe


AutoMAX CK - NAC IFCC METHOD


AVNAC (A) -100 2 x 50 ml

AVNAC (A) -200 4 x 50 ml

(R1 : 2x40ml, R2 : 20ml)

(R1 : 4x40ml, R2 :4x 10ml)

Salient Features :


2. Two Liquid Reagents (4 parts R1+1 part R2)3. Linearity 1500 IU/L.4. Measuring wavelength 340 nm.5. Results by calibration with commercial calibrators OR by Kinetic factor 4127 at 340 nm at 37° C.6. Programme sheets available for different analyzers.

AutoMAX CREATININE MODIFIED JAFFE’S METHOD


AVCRE (A) - 200 4 x 50 ml

AVCRE (A) - 400 8 x 50 ml

AVCRE (A) - 800 16 x 50 ml

(R1 : 4x40ml, R2 :2x 20ml)

(R1 : 8x40ml, R2 :4x 20ml)

(R1 : 16x40ml, R2 :8x 20ml)

Salient Features :


2. Two Liquid Reagents.(4 parts R1+1 part R2).3. Linearity 25 mg/dl.4. With Lipid Clearing Factor (LCF).5. No interference from Bilirubin up to 25 mg/dl, Hemoglobin up to 22 gm/dl.6. Aqueous calibrator provided.7. Programme sheets available for different analyzers.

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AutoMAX GLUCOSE (GOD - POD METHOD)


AVGLU (A) - 500 500 ml

AVGLU (A) - 1000 1000 ml

Salient Features :


2. Two Liquid Reagent.3. One step End Point assay.4. Linearity: 1000 mg/dl 5. With Lipid Clearing Factor (LCF) 6. Aqueous calibrator provided.7. Programme sheets available for different analyzers.

LiquiMAX HDL CHOLESTEROL -DIRECT (HOMOGENOUS/DETERGENT SELECTION METHOD)


AVHDL(DA)-160 160 ml

AVHDL(DA)-320 320 ml

(R1 : 4 x30 ml, R2 :2 x 20 ml)

(R1 : 4 x60 ml, R2 :4 x 20 ml)

Salient Features :

1. Two Liquid Reagents with Calibrator.2 End Point/Fixed Time procedures can be performed.3. Linearity range 3.7-200 mg/dl.4. No offline pre treatment of serum samples required5. Results correlate with other reference methods. 6. Meets NCEP guidelines.7. Works well with fasting & non fasting patient samples.8. Precision with high triglyceride samples.9. Can be used on any spectrophotometer, discrete semi automated and automated analyzers.

LiquiMAX LDL CHOLESTEROL- DIRECT (HOMOGENOUS/DETERGENT SELECTION METHOD)

Salient Features :

1. Two Liquid Reagents with Calibrator.2 End Point/Fixed Time procedures can be performed.3. Linearity range 6.6-1250 mg/dl.4. No offline pre treatment of serum samples required 5. Meets NCEP guidelines.6. Correlation with gold standard Beta quantification & Immuno separation.7. Overcomes critical limitations of Friedewald formula.8. Works well with fasting & non fasting patient samples.9. Precision with high triglyceride samples.10.Can be used on any spectrophotometer, discrete semi automated and automated analyzers


AVLDL(DA)-160 160 ml

AVLDL(DA)-320 320 ml

(R1 : 4 x30 ml, R2 :2 x 20 ml)

(R1 : 4 x60 ml, R2 :4 x 20 ml)

LiquiMAX MICRO PROTEIN (PYROGALLOL RED METHOD)

Salient Features :1. Single Liquid Reagent.2. Linearity : 250 mMol/L.3. 5 minutes End Point assay4. Results correlate with Benzethonium Chloride method.5. Tailor made for tropical Conditions.

6. Superior over sulphosalicylic acidod.

7. Detects Microprotein as low as 4 mg/dt

6. Incorporates Six Sigma methodologies throughout the manufacturing processes where in

the product under goes various stringent process checks like Defining, Measuring,

Analyzing, Improving and Controlling. (DMAIC)

7. No interference was observed by ascorbic acid up to 20 mg/dl,


AVMPR-50 2 x 25 ml

AVMPR-100 4 x 25 ml









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AutoMAX TOTAL PROTEIN BIURET METHOD


AVTPT (A) - 200 4 x 50 ml

AVTPT (A) - 400 8 x 50 ml

Salient Features :


2. Single Liquid Reagent.3. One step End Point assay5. With Lipid Clearing Factor (LCF)6. Linearity 10 gm/dl.7. Aqueous protein calibrator provided.8. Programme sheets available for different analyzers.

AutoMAX SGOT(AST) IFCC METHOD


AVGOT (A) -200 200 ml

AVGOT (A) -400 400 ml

AVGOT (A) -800 800 ml

(R1 : 4x40ml, R2 : 2x20ml)

(R1 : 8x40ml, R2 : 4x20ml)

(R1 : 16x40ml, R2 : 8x20ml)

Salient Features :


2. Two Liquid Reagents (4 parts of R1 + 1 part of R2).3. Linearity 1000 IU/L.4. Measuring wavelength 340 nm.5. Results by calibration with commercial calibrators OR by Kinetic factor 1746 at


AutoMAX SGPT (ALT) IFCC METHOD


AVGPT (A) -200 200 ml

AVGPT (A) -400 400 ml

AVGPT (A) -800 800 ml

(R1 : 4x40ml, R2 : 2x20ml)

(R1 : 8x40ml, R2 : 4x20ml)

(R1 : 16x40ml, R2 : 8x20ml)

Salient Features :


2. Two Liquid Reagents (4 parts of R1 + 1 part of R2).3. Linearity 1000 IU/L.4. Measuring wavelength 340 nm.5. Results by calibration with commercial calibrators OR by Kinetic factor 1746 at


AutoMAX PHOSPHORUS MOLYBDATE-UV METHOD


AVPHO (A) - 200 4 x 50 ml

Salient Features :


2. Single Liquid Reagent.3. One step End Point assay.4. Linearity 20 mg/dl.5. No deproteinization of the sample required6. Superior over Phenyl hydrazine and Amino naphtho sulphonic acid methods7. With Lipid Clearing Factor (LCF).8. Aqueous calibrator provided.9. Programme sheets available for different analyzers.




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AutoMAX URIC ACID URICASE METHOD


AVURI (A) - 200 4 x 50 mlAVURI (A) - 400 8 x 50 mlAVURI (A) - 800 16 x 50 ml

Salient Features :


2. Single Liquid Reagent.3. Linearity 30 mg/dl.4. With *TBHBA as Chromogen. (*TBHBA = 2,4,6 Tribromo 3 Hydroxy Benzoic Acid).5. With Lipid Clearing Factor (LCF).6. One step End Point Assay.8. Aqueous calibrator provided.9. Programme sheets available for different analyzers.

AutoMAX URIC ACID URICASE METHOD


AVURI (A) - 200 4 x 50 mlAVURI (A) - 400 8 x 50 mlAVURI (A) - 800 16 x 50 ml

Salient Features :


2. Single Liquid Reagent.3. Linearity 30 mg/dl.4. With *TBHBA as Chromogen. (*TBHBA = 2,4,6 Tribromo 3 Hydroxy Benzoic Acid).5. With Lipid Clearing Factor (LCF).6. One step End Point Assay.8. Aqueous calibrator provided.9. Programme sheets available for different analyzers.

AutoMAX UREA-GLDH UREASE-GLDH METHOD


AVURE (A) - 200 200 ml

AVURE (A) - 400 400 ml

AVURE (A) - 800 500 ml

(R1 : 4x40ml, R2 :2x 20ml)

(R1 : 8x40ml, R2 :4x 20ml)

(R1 : 16x40ml, R2 :8x 20ml)

Salient Features :


2. Two Liquid Reagents( 4 parts R1 + 1 part R2).3. UV-Fixed Time (Initial Rate) Method.4. Linearity 350 mg/dl.5. BUN values can be estimated 6. Aqueous calibrator provided.7. Programme sheets available for different analyzers.

AutoMAX TRIGLYCERIDES GPO - PAP TRINDERS METHOD


AVTGL (A) - 200 4 x 50 ml

AVTGL (A) - 400 8 x 50 ml

AVTGL (A) - 800 16x 50 ml

Salient Features :


2. Single Liquid Reagent.3. Linearity 1200 mg/dl.4. With*TBHBA as Chromogen (*2,4,6-Tribromo-3-hydroxy-benzoic acid).5. One step End Point Assay.7. Aqueous calibrator provided.8. Programme sheets available for different analyzers.










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SeroMAX ASO LATEX SLIDE AGGLUTINATION METHOD


AVASO - 25 25 TESTS

AVASO - 50 50 TESTS

Salient Features :

1. Cut off sensitivity 200 IU/ml.2. Homogenous latex particles.3. Qualitative and Semi quantitative procedures.4. Positive and Negative Controls provided.5. Sample dilution is not required.6. Sensitivity 200 IU/ml is calibrated against WHO calibrators.7. Overcomes Prozone Effect and Hook Effect.

SeroMAX CRP LATEX SLIDE AGGLUTINATION METHOD


AVCRP - 25 25 TESTS

AVCRP - 50 50 TESTS

AVCRP - 100 100 TESTS

Salient Features :

1. Cut off Sensitivity 0.6 mg/dl.2. Uniform and Homogeneous Latex Particles ensure clear Agglutination.3. Qualitative and Semi quantitative procedures.4. Positive and negative controls provided.5. Sample dilution is not required.6. Sensitivity 0.6 mg/dl is calibrated against WHO calibrators.7. Overcomes Prozone Effect.

SeroMAX RA LATEX SLIDE AGGLUTINATION METHOD


AVRAF - 25 25 TESTS

AVRAF - 50 50 TESTS

AVRAF - 100 100 TESTS

Salient Features :

1. Cut off sensitivity 12 IU/ml.2. Uniform and Homogeneous Latex Particles ensure clear Agglutination.3. Qualitative and Semi quantitative procedures.4. Positive and negative controls provided.5. Sample dilution not required.6. Sensitivity 12 IU/ml is calibrated against WHO calibrators.7. Overcomes interferences like Prozone Effect and Hook Effect.

SeroMAX RPR SLIDE AGGLUTINATION METHOD


AVRPR - 50 50 TESTS

AVRPR - 100 100 TESTS

AVRPR - 500 500 TESTS

Salient Features :

1. Uniform, homogenous, micronised carbon particles (Cardiolipin Antigen).2. Cardiolipin Antigen is in aqueous base.3. Qualitative and Semi quantitative procedures.4. Positive and negative controls provided.5. Sample dilution not required.6. Sample inactivation not required.7. Overcomes interferences like Prozone Effect and Hook Effect.A

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SeroMAX

SeroMAX WIDAL AGGLUTINATION METHOD


AVWID - 20 4 x 5 ml

Salient Features :

1. Separate colour coded antigens.2. Uniform, homogenous and stabilized bacterial antigens.3. Qualitative and Semi quantitative slide test and tube test procedures.4. Positive control provided.5. Sample dilution not required.6. Overcomes interferences like Prozone Effect and Hook Effect .

SeroMAX WIDAL (OH) AGGLUTINATION METHOD


AVWID(OH) - 20 2+2 x 5 ml

Salient Features :

1. Separate colour coded antigens.2. Uniform, homogenous and stabilized bacterial antigens.3. Qualitative and Semi quantitative slide test and tube test procedures.4. Positive control provided.5. Sample dilution not required.6. Overcomes interferences like Prozone Effect and Hook Effect .

SeroMAX ANTI ABD (COMBI PACK) AGGLUTINATION METHOD


AVABD - 15 3 x 5 ml

AVABD - 30 3 x 10 ml

Salient Features :

1. Uniform, homogenous and stabilized bacterial antigens.2. Qualitative and Semi quantitative slide test and tube test procedures.3. Contamination due to HIV, HBsAs & HCV is practical excluded and safe to use.




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TurbiMAX ASOIMMUNO TURBIDOMETRIC METHOD


AVASO (T) - 50 50 ml

AVASO (T) -100 2 × 50 ml

Salient Features :1. Quantitative Immunoturbidometric assay.

2. Two liquid stable reagents(Turbilatex and Diluent)

3. Linearity range 800 IU/ml.

4. Calibrator provided.

5. No Prozone effect was detected upon 3000 IU/mL.

6. No interference from Hemoglobin (10 g/l), Bilirubin (20 mg/dl), Lipemia (10 g/l) and Rheumatoid factors (600IU/mL).

7. Can be automated to semi and fully auto analyzers.

TurbiMAX CRPIMMUNO TURBIDOMETRIC METHOD


AVCRP (T) - 50 50 ml

AVCRP (T) -100 2 × 50 ml



3. Linearity range 100 mg/dl.

4. Detects as low as 2 mg/dl



6. No interference from Bilirubin (20 mg/dl), Lipemia (10 g/l) and Rheumatoid factors (300 IU/mL).

8. Can be automated to semi and fully auto analyzers

TurbiMAX RA IMMUNO TURBIDOMETRIC METHOD


AVRAF (T) - 50 50 ml

AVRAF (T) -100 2 × 50 ml



3. Linearity range 20-160 IU/ml.

4. Detects as low as 6 IU/ml.



7. No interference from Hemoglobin (10 g/l), Bilirubin (20 mg/dl), Lipemia (10 g/l)

8. Can be automated to semi and fully auto analyzers.

TurbiMAX APOLIPOPROTEIN (A1) IMMUNO TURBIDOMETRIC METHOD


AVAPL (A1) - 50 50 ml

AVAPL (A1) - 100 2 x 50 ml

Salient Features :1. Photometric quantitative assay.

2. Liquid stable reagents(Turbilatex and Diluent)

3. Linearity range 30-270 mg/dl



6. No Prozone effect.

7. Bilirubin,Hemoglobin and Lipemia do not interfere


Six Sigma Immuno Turbidometry

TurbiMAX





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TurbiMAX MICROALBUMINIMMUNO TURBIDOMETRIC METHOD


AVMAL (T) - 50 50 ml


2. Liquid stable reagents(Turbilatex and Diluent)

3. Linearity range 150 IU/ml.

4. Detects as low as 2 ms/L.


6. No Prozone effect was detected upon 1000 mg/L.

7. No interference from Bilirubin (10 gm/L), Creatinine (3 gm/L) and Glucose (2 gm/L)


TurbiMAX APOLIPOPROTEIN (B)IMMUNO TURBIDOMETRIC METHOD


AVAPL (B) - 50 50 ml



3. Linearity range 40-800 mg/dl



6. No Prozone effect.

7. Bilirubin,Hemoglobin and Lipemia do not interfere


TurbiMAX LIPOPROTEIN(a) IMMUNO TURBIDOMETRIC METHOD


AVLPA (T) - 50 50 ml


2. Lliquid stable reagents(Turbilatex and Diluent)

3. Linearity range 90 mg/dl

4. Detects as low as 1.5 mg/dl



7. No interference from Hemoglobin (5 g/l), Bilirubin (20 mg/dl), Plasminogen (680 mg/dL), Ascorbic acid (200 mg/dL) Lipemia (20 g/l) and Rheumatoid factors (100IU/mL).


Six Sigma Immuno Turbidometry

TurbiMAX




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AVPTT - 5 5 ml

AVPTT - 60 12 x 5 ml

Salient Features :1) Ready to use Calcium Thromboplastin Reagent.

2) Serum sample at random can be tested (Any time serum sample)

3) Reagents can be tested manually and are adaptable to coagulation analyzers.

4) INR conversion table provided.

5) Lot specific ISI values assigned.

6) Meets the guide lines of ICSH and ICHT

APTT ...


AVAPT - 3 3 ml

AVAPT - 36 12 x 3 ml

Salient Features :

FIBRINOGEN ...


AVFIB - 3 3 ml

AVFIB - 36 12 x 3 ml

Salient Features :

Six Sigma Coagulation




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Ref./Cat. No.

AVPRE (S) - 100

AVPRE (C) - 50

100 Tests

50 Tests

Salient Features :

MaxLine/ MaxView PREGNANCY STRIP /

1. Lateral Flow Immuno Chromatography.

2. Sensitivity 25 mIU/ml hCG in urine.

3. No cross reaction with LH upto 500 mIU/ml, FSH upto 1000 mIU/ml & TSH upto 1000 mIU/ml

4. Available as 3mm, 3.5mm & 4mm strips.

5.

CASSETTE

Available as 3mm & 4mm cassettes.

MaxLine HIV 1/2 AB Cassatte

Ref./Cat. No.

AVHIV - 10

10 Tests

AVHIV - 40

40 Tests

Salient Features :


2. Detects HIV 1 and HIV 2 simultaneously.

3. Differential diagnosis (separate lines for HIV 1 & HIV 2).

4. Detects HIV 1 ‘O’ sub type.

5. Sensitivity - 99.4 - 100 %.

6. Specificity - 99.8 to 99.9 %

7. Accuracy - 99.6 - 99.9 %

MaxLine HCV Cassette

Ref./Cat. No.

AVHCV - 10

10 Tests

AVHCV - 40

40 Tests

Salient Features :


2. Sandwich Immuno Assay.

3. Relative sensitivity - 96.8%.

4. Relative specificity - 99%

5. Overall Accuracyt - 98.9%

MaxLine HBsAg Strip/ Cassette

Ref./Cat. No.

AVHBV (S) - 100

100 Tests

AVHBV (C) - 40

40 Tests

Salient Features :


2. Available as strips & cassettes format.

3. Specificity - 99 %

Six Sigma Rapid Tests

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MaxLine DENGUE

Ref./Cat. No.

AVDEN - 10

AVDEN - 40

10 Tests

40 Tests

Salient Features :


2. Detects IgM & IgG simultaneously.



5. Relative specificity - 100%

6. Overall agreement - 99.3%

MaxLine MALARIA (ANTIGEN)

Ref./Cat. No.

AVMAL (1) - 10

AVMAL (1) - 50

10 Tests

50 Tests

Salient Features :


2. Detects palciparum malaria & the malaria caused by other species.

3. Sandwich Immuno Assay, storage at RT

4. Relative sensitivity - 100%.

5. Relative specificity - 98.6%


MaxLine MALARIA (ANTIBODY)

Ref./Cat. No.

AVMAL (2) - 10

AVMAL (2) - 50

10 Tests

50 Tests

Salient Features :






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MaxLine TUBERCULOSIS

Ref./Cat. No.

AVTUB - 10

AVTUB - 40

10 Tests

40 Tests

Salient Features :


2. Detects all kinds of antibodies (IgM, IgG & IgA).





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InstantView TROPONIN - I

InstantView TROPONIN - I

Ref./Cat. No.

AVTRO - 10

AVTRO - 30

10 Tests

30 Tests

Ref./Cat. No.

AVTRO - 10

AVTRO - 30

10 Tests

30 Tests

Salient Features :


2. FDA 510 (k) cleared.

3. CE marked.

4. Sensitivity 1.5 ng/mL,TnL

5. Buitt in Control features.

Salient Features :


2. FDA 510 (k) cleared.

3. CE marked.

4. Cut off sensitivity 0.9 - 1.5 (different patient groups).

MaxLINE TROPONIN I (WHOLE BLOOD)

Salient Features :


2. Sensitivity 99.3%

3. Specificity 96.0%

addition

Ref./Cat. No.

AVMLTRO - 10

AVMLTRO - 30

10 Tests

30 Tests

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MaxLine SYPHIILIS Strip/ Cassette

Ref./Cat. No.

AVSYP (S) - 100

AVSYP (C) - 40

100 Tests

40 Tests

Salient Features :


2. Available as strips & cassettes format.

5. Relative sensitivity - 99.6% (98.6 - 100%)

6. Relative specificity - 99.6% (98.6 - 100%)

7. Overall accuracy - 99.9% (99 - 99.9 %)

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AVBGM 1 unit

AVBGM (S) 50 Nos.

Salient Features :1. Advanced Bio Sensor Technology.

2. Average Test Time - 5 seconds.

3. Memory Capacity - last 500 test data.

4. Easy Code setting with Code Card.

5. Data downloading capability to PC (optional).

6. Human Voice data telling function (optional).

1. Test strips available as 50 test pack (to be supplied separately).

Six Sigma Instrument

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A complete range of imported micro pipettes specially designed and crafted for fatigue free pipetting comfort are made available from Avecon to ensure highest level of precision, accuracy and reliability.

AVPTF-10 MICROPIPETTE Fixed 10 µL.





AVPTV-10 MICROPIPETTE Variable 1 - 10 µL.




AVPTV-10000 MICROPIPETTE Variable 1 - 10 ml.

Ref./Code Name of the Product Type Volume

Six Sigma Micropipettes

OEM AND CUSTOM MANUFACTURING

SUCCESSFUL PARTNERSHIPS YIELD SUCCESSFUL RESULTS - It's all about ‘WIN-WIN’ situation.

Proven Experience

Technology Development and Transfer :

Proven Manufacturing

“Successful products stem from successful partnerships”. We firmly believe in this ideology. That is why whenever we deal with any OEM partners for their outsourcing and custom manufacturing needs we fully cooperate with them. It is imperative that there is understanding, trust and confidence built between our partners and us. In short, It's all about the right relation ship. From the initial product concept to its development, launch and commercialization we know what is expected and required – you can count on us

We are now capable of providing quality products, services, knowledge, and expertise to the diagnostic and life science industries. With the clear focus of becoming recognized leader in this field, we are in the main track of establishing our relationships with several domestic/overseas partners for their outsourcing needs. Every day, our current and new potential partners are approaching us with unique and cost effective product categories.

Our technical team is continuously putting relentless efforts to expand our product portfolio and at the same time keeping the quality of our IVD products at the highest level by regular value additions and perfective maintenance. The main activities are in line with our core competence in the field of Clinical Chemistry and we are now able to offer many of the ultra stable, ready to use clinical chemistry reagents that are capable of setting bench marks

Our talented and experienced research team can develop the technology for any complex product in the core competent areas like Clinical Chemistry, Serology, Immuno Assays, Rapid tests, Monoclonal Antibodies and Mammalian Cell Culture as per the requirements of the customer. Upon the successful completion of the product development, the technology will be transferred to the customer. In this particular activity we are very committed that, the genuine technology is developed and transferred to the customer at a reasonable royalty.

We have constructed an outstanding state-of-the-art GMP facility for the development as well as for the manufacturing of Clinical chemistry, Serology and Immuno assay reagents and our validated GMP manufacturing unit has the facilities for the following :

Sophisticated R & D and QA laboratories Liquid Formulation & FillingLyophilization Powder Blending & Filling Rapid Test Development and Manufacturing Immuno Assay Development and ManufacturingPackaging Design Labeling Kit Assembly OEM/Custom Formulations Instrument Applications Regulatory/Documentation

Technology Development and Transfer.

Six Sigma

Proven Quality

Proven Compliance

Proven Support

Let us help you to help us

Organizational Activities

AVECON

Our quality control system encompasses a comprehensive and exhaustive series of stringent quality checks (Visual, Chemical and Bacteriological). The inspection at various stages of the production cycle begins with constant surveillance of raw materials, their testing, vendor assessment, Intensive in process checks. The systems are well documented meticulously as per the quality norms which guarantee lot-to-lot consistency and specific product performance time after time, after time.

In addition to achieving total product quality, we intend to make our manufacturing processes compliant to various regulatory certifications like ISO 9002, CE and FDA. Quality, consistency and documented performance are given top priority at Avecon. Our facilities are also subject to audit and inspection by several Govt regulatory agencies like State and Central Drug Control Authorities and Indian FDA.

Our commitment to the business runs deep in terms of involvement, support and resource dedication. We truly recognize that, to provide complete solutions to customers' outsourcing needs our support must be an integral part of the commitment. Our team with extensive IVD industry experience is relentlessly working towards understanding customers' needs and their product specifications. Our team addresses those requirements in time, within the specifications and budget.

To obtain additional information, or to discuss potential business opportunities, please contact us at [email protected] web: www.aveconhealthcare.com

(A schematic diagram)

OEM AND CUSTOM MANUFACTURING

Researchand

Development

CUSTOMERNEEDS

TechnicalSupport

QualityAssurance

andQualityControl

Manufacturing

PackageDesign

andKit

Assembly

Distributionand

LogisticsSales,

Marketing,CustomerSupport

RegulatoryAffairs

Focus

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Six Sigma

Six Sigma

1. Single order of Rs. 10000/- or more at a time will be supplied FOR destination

2. All the products are carefully checked and properly packed at the time of dispatch. No claims are accepted for

breakage, leakage, damages and loss that are occurring due to transit lapses.

3. All the products are dispatched at consignee’s risk, however they can be insured on demand at customer’s cost.

4. All the supplies to the authorised distributors shall be made as per the terms of distributor’s agreement.

5. Prices and Specification can be changed without any prior notice.

Declaration :

All our products are for in vitro diagnostic use only. AVECON will not be responsible, if they are used for any

other purposes.

Warranty :

All the products are assured for quality. If the customer is not satisfied with product’s performance, he may return them

with possible reasons and appropriate documents. The replacement can be given only after evaluation of such

products at our Q.A. Lab.

TERMS & CONDITIONS

DISTRIBUTION & LOGISTICS

Avecon Healthcare Pvt. Ltd. has a network of local, regional, national and international distributors. In

cooperation with our distributor partners, we are able to provide diagnostic products, services and support to

clinical laboratories from the smallest laboratory to the biggest Corporate Hospitals and Nursing Homes.

• For general queries please contact Avecon’s Information Bureau at :

• For sales, pricing and business collaborations etc please contact Avecon’s Sales Team at :

• For technical details, queries & complaints if any please contact Avecon’s Technical Department at

• For distribution & Logistics please contact Avecon’s Administration Group at :

• For any service lapses and resolved queries please contact Avecon’s Help Desk at

• For export queries please contact Avecon’s Export Division at :

[email protected]

[email protected]

[email protected]

[email protected]

[email protected]

[email protected]

:

PLANT AND OFFICE :

AVECON HEALTHCARE PVT.LTD.

# 338, Sector-2, Industrial Growth Centre, Saha - 133104. (INDIA)

www.aveconhealthcare.com

Plant : # 338, Sector-2, Industrial Growth Centre, Saha-133104.Ph : 0171-3248775 - 76, Website : www.aveconhealthcare.com

E-mail : [email protected], [email protected]

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