medical instruments catalogue - kanggaoteen.kanggaote.com/static/upload/medical instruments... ·...

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Instruments & Equipment

Medical Instruments Catalogue

Beijing Kanggaote Instruments and Equipments Co.Ltd


Company profile

BeiJing KANGGAOTE Instruments & Equipment Co., Ltd. (short for Beijing KANGGAOTE )was established

in September 2008 and engaged in the sales of portable instruments .

We are the first company which can supply the one-stop service in the filed . We have large customers

base such as State Grid,China Southern Power ,Grid,subway,High-speed train, EMU ,Environmental

Protection Agency,PetroChina,Sinopec,Colleges and universities,CNNP,CNPC,SGCC,China CDC,MEP

and other world-famous companies and government agencies.

We can provide a series of professional one-stop service such as pre-sale technical support,product

selection,product training,after-sales repair,complete solution etc.

Beijing KANGGAOTE is growing with a high speed since the establishment, we are making great strides in

development. Now we are the authorized dealers of more than 20 international first-line brands.With the

detailed product database and by virtue of the service innovation in the field of network marketing and

channel management, as well as the advantage in the information processing technology ,we provide a

professional and low-cost trading platform for the manufactures and customers.

Recently the world is suffering the outbreak of COVID-19,Our company promptly coordinates the supply

and Now we have sold over 300,000 units masks and overalls abroad.We have cooperated with DACH,-

CLIMAX and LANAFORM,etc and provided the pretective goods to other countries.The global fight against

the epidemic, we are in action.

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Instruments & EquipmentsDisposable face mask

Composition Disposable face mask is made of non woven fabric, breathable and soft, with excellent filtration;odorless, skin-friendly, latex and fiberglass free.Bacterial filtration: BFE 95% - 99%With flexible nose clipon

Size 17.5x9.5cm, 16.5x9.5cm, 17.5x9cm, 18x9cm; for adult and children use.

Specification Top Layer-20 GSMMiddle Layer-18 GSMBottom Layer-20 GSM

Type 2 earloops, 4 ties, with a face shield.

Layer 2-ply, 3-ply, 4-ply, 6-ply, etc.

Color white, green, blue, pink, yellow, etc.

Packing 5 to 10 pcs/pack, 50 pcs/box

Beijing Kanggaote Instruments and Equipments Co.Ltd Email: [email protected]:0086-13810851425

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Qual i ty Assurance：Test ing Report and CE Cert i f icate

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Instruments & Equipments

Particulate Respirator KN95 (GB2626)


Product Name

Performance Standard

Type

Model

Protection Grade

Component

Function and application

Instructions

Caution

Storage

Expiration date

Particulate Respirator KN95

GB2626-2006

Respiratory protective product

RZ95B

KN95

Mask body, nose clip and ear loops.

Used for protection against virus. It can protect you from dust, droplets, saliva and bacteria.

Hold the mask by the ear loops. Place a loop around each ear and pinch the nose clip to the shape of your nose.

1.Do not use when expired.2.Do not wash or disinfect, avoid repeated use and destroy after use.3.Do not use if the package is damaged. 4.Not suitable for people sensitive to non-woven fabric.5.Please refer to the instructions before use.

Stored at room temperature with good ventilation, non-corrosive environment and no more than 80% relative humidity. Avoid high temperature.

36 months in the correct storage environment.

Qual i ty Assurance：CE Cert i f icate and FDA Medical Device Registrat ion

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Particulate Respirator KN95 (GB2626)

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Protective OverallCK-1

Email: [email protected]:0086-13810851425

Categorization Protection class: Type 3.

Productdescription

The CK1 consists of a body piece, long sleeves, long trouser legs and a hood,attached with an overlock-seam and a zipper cover strip. The zipper covers the chin and the neck areas. The cut of the coverall is designed for more mobility. The coverall is equipped with an overlock-seam bordered elastic strap at the face, arm, leg,and waist. Material: SMMS.

Material

Applied standards

SMMS 60g

EN 14126:2003,EN 14325:2001, ISO/FDIS 16603 and ISO/FDIS 16604, ISO/DIS 22611 and ISO/DIS 22622, EN 340, Type 3:EN466

Application This coverall offers protection against dangerous substances and contamination. It can be used, depending on the circumstances and degree of the toxicity, against air carried particles and nontoxic splashes and spray

For general isolation of outpatient/ward/laboratory in medical institutions

For civil protection such as security inspection/disinfection/sentry box


Categorization Protection class: Type 3，Type 4

Productdescription

The CK2 is sterilized by irradiation,and the sterilization period is one month.It can be used by hospital medical staff and also can be used in ICU.It is also waterproof,breathable,super abosorbent,wear-resistant,physiological comfortable and virus resistant.

Material

Applied standards

The CK-2 is mainly made of high barrier composite non-woven fabric,which is continuously flocculent and dose not produce dust.

EN14605:2005+A1:2009EN14126:Type3,Tpye4


Detailed Technology

Sealed pressure

adhensive tape

armpit

Sealed pressure

adhensive tape

riseand crotch

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Strong sealed brim elastane tape

Fly-prssure-sensitive adhensive tape

Pressure adhensive tape waist movecomfortable

Categorization Protection class: Type 5，Type 6

Productdescription

The CK3 is designed for more mobility. The coverall is equipped with an overlock-seam bordered elastic strap at the face, arm, leg,and waist.

Material

Applied standards

The CK-3 is mainly made of high barrier composite non-woven fabric,which is continuously flocculent and dose not produce dust.

EN14605:2005+A1:2009EN13982:Type5EN13034:Type6


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Isolation Gown


Isolation Gown is made of non woven fabric and SMS fabric, soft and skin-fnendly.

Used in hospital, aboratory to prevent and isolate dust partice, alcohol, bood, bacteria

and virus invading.

Matenal: non woven fabnc (classic gown), MS fabric (premium gown), reinforced gown.

Cuff: knitted cuff, elastic cuff.

With 2 waist belts, 2 neck belts (or velcro belts)

Color:white,green,blue, pink, yellow. etc.

Size:115x137cm,120x140cm. 130x150cm, 140x60cm, S,M,L,XL,XXL

Packing: 1 piece in a sterile pouch, 50 pcs/carton

Sterile by EO gas if need.

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Single-use latex exam gloves


Single-use latex exam gloves(sterile/non-sterile)(lightly powdered/powder free)

Use: public medical, food manufecturing etc.

Property: soft, suitable for wear.

Size: S. M. L.

Packing: 100 pairs/box, 10 boxes/carton.

100 pac/box, 10 or 20 boxes/carton.

Carton size: 61x22x44.5CM

52x26.5X33CM

Qual i ty Assurance CE compl iant

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SARS-CoV-2 Antibody Test(Lateral Flow Method)Catalog No.: W195

INTENDED USE

Wondfo SARS-CoV-2 Antibody Test (Lateral Flow Method) is an immunochromatographic assay for rapid, qualitative detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) IgG/IgM antibody in human whole blood, serum or plasma sample. The test is to be used as an aid in the diagnosis of coronavirus infection disease (COVID-19), which is caused by SARS-CoV-2.

The test provides preliminary test results. Negative results don’t preclude SARS-CoV-2 infection and they cannot be used as the sole basis for treatment or other management decision.

For in vitro diagnostic use only. For professional use only.

SUMMARY

On December 31, 2019, several cases of pneumonia in Wuhan City, Hubei Province of China were reported to the World Health Organization (WHO). The novel virus, now known as SARS-CoV-2 (previously known as 2019-nCoV), a RNA virus of the beta coronavirus family, has since spread across China and to other countries and territories. The WHO has named the disease caused by SARS-CoV-2 as coronavirus disease 2019 (abbreviated “COVID-19”).

PRINCIPLE

Wondfo SARS-CoV-2 Antibody Test (Lateral Flow Method) is based on the principle of capture immunoassay for determination of SARS-CoV-2 IgG/IgM antibodies in human whole blood, serum and plasma. When the specimen is added into the test device, the specimen is absorbed into the device by capillary action, mixes with the SARS-CoV-2 antigen-dye conjugate and flows across the pre-coated membrane.

When the SARS-CoV-2 antibodies level in the specimen is at or above the target cutoff (the detection limit of the test), the antibodies bound to the antigen-dye conjugate are captured by anti-human IgG antibody and anti-human μ chain antibody immobilized in the Test Region (T) of the device, and this produces a colored test band that indicates a positive result. When the SARS-CoV-2 antibody level in the specimen is zero or below the target cutoff, there is not a visible colored band in the Test Region (T) of the device. This indicates a negative result.

To serve as a procedure control, a colored line will appear at the Control Region (C), if the test has been performed properly.

PRECAUTION

1. This kit is for in vitro diagnostic use only.2. All specimens should be treated as capable of transmitting

diseases. Use appropriate precautions in the collection, handling, storage and disposal of patient samples and used kit contents. And follow biosafety level 2 or higher guidelines.

3. Wear appropriate personal protective equipment (e.g. gowns, gloves, eye protection) when handing the contents of this kit.

4. Proper specimen collection storage and transport are critical to the performance of this test.

5. Discard after first use. The test cannot be used more than once.6. Do not touch the reaction area of test strip.7. Do not use test kit beyond the expiration date.8. Do not use the kit if the pouch is punctured or not well sealed.9. Testing should be applied by professionally trained staff working in

certified laboratories or clinics at which the sample(s) is taken by qualified medical personnel.

10. The test result should be interpreted by the physician along with clinical findings and other laboratory test results.

11. DISPOSAL OF THE DIAGNOSTIC: All specimens and the used-kit has the infectious risk. The process of disposing the diagnostic must follow the local infectious disposal law or laboratory regulation.

MATERIAL

Material Provided1. 20 Individual sealed pouches, each pouch contains:

■ 1 x Test cassette■ 1 x Desiccant pouch

2. 20 disposable droppers3. Detection buffer (1*6 mL)4. Instructions for use

Material Required but Not Provided1. Specimen Collection Containers2. Centrifuge (for serum/plasma sample)3. Timer4. Personal protective equipment, such a protective gloves, medical

mask, goggles and lab coat.5. Appropriate biohazard waste container and disinfectants.

STORAGE AND STABILITY

1. Store at 2~30ºC in the sealed pouch up to the expiration date printed on the package. Do not freeze.

2. The test cassette should be used within 1 hour after taking out from the foil envelope. Buffer solution should be re-capped in time after use.

3. Keep away from sunlight, moisture and heat.4. Kit contents are stable until the expiration date printed on the outer

box.

SPECIMEN COLLECTION AND PREPARATION

The test can be performed with whole blood, serum and plasma.

For whole blood:1. Using standard phlebotomy procedure, collect a venipuncture

whole blood specimen using a blood collection tube with suitable anticoagulant (containing EDTA, Heparin or Citrated sodium). Other anticoagulants have not been validated and may give incorrect result.

2. It is recommended that whole blood specimen is tested at the time of specimen collection. If the specimens are not tested immediately, they may be stored at 2ºC～8ºC for up to 7 days. Prior to testing, mix the blood by gentle inversion several times, do not freeze or heat whole blood specimens.

For Serum and Plasma:1. Using standard phlebotomy procedure, collect a venipuncture

whole blood specimen using a blood collection tube. If collecting plasma use a blood collection tube containing suitable anticoagulant (containing EDTA, Heparin or Citrated sodium). Other anticoagulants have not been validated and may give incorrect result.

2. Centrifuge whole blood and separate the plasma from red blood cell as soon as possible to avoid hemolysis.

3. Test should be performed within 8 houres after the specimens have been collected. Do not leave the specimens at room temperature for prolonged periods. Serum or plasma specimens may be stored at 2ºC～8ºC for up to 3 days prior to testing. Serum or plasma specimens may be stored at -20ºC for up to 9 days.

Note: Bring specimens to room temperature before testing. Frozen specimens must be completely thawed and mixed well prior to testing. Specimens should not be frozen and thawed repeatedly. Severe hemolytic or heat-inactivated specimens are not recommended.

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TEST PROCEDURE Please read the instruction for use carefully before performing the test.1. Allow the device, buffer and specimen to equilibrate to room

temperature (10ºC ～30ºC) prior to testing.2. Remove a test cassette from the foil pouch by tearing at the notch

and place it on a level surface.3. Transfer 10 μL of whole blood or serum or plasma specimen to the

sample well (small well) and then add 2-3 drops (80 μL) of buffer solution to the buffer well (large well).

4. As the test begins to work, you will see purple color move across the result window in the center of the test device.

5. Wait for 15 minutes and read the results. Do not read results after 20 minutes.

Note: the rightmost window on the cassette shows the product abbreviation “nCoV” to identify this product.

RESULT INTERPRETATION

Positive Result

Colored bands appear at both test line (T) and control line (C). It indicates a positive result for the SARS-CoV-2 antibodies in the specimen.

Negative Result

Colored band appear at control line (C) only. It indicates that the concentration of the SARS-CoV-2 antibodies is zero or below the

nCoV nCoV nCoVnCoV nCoV nCoVnCoV nCoV nCoV

CT

SARS-C

oV-2

nCoV nCoV nCoVnCoV nCoV nCoVnCoV nCoV nCoV

CT

SARS-C

oV-2

10μL 2~3 Drops

detection limit of the test.

Invalid Result

No visible colored band appear at control line after performing the test. The directions may not have been followed correctly or the test may have deteriorated. It is recommended that the specimen be re-tested.

QUALITY CONTROL

A procedural control is included in the test. A colored line appearing in the control region (C) is considered an internal procedural control. It confirms sufficient specimen volume, adequate membrane wicking and correct procedural technique.

Good laboratory practice recommends the use of the control materials. Users should follow the appropriate federal state, and local guidelines concerning the frequency of assaying external quality control materials.

3. The accuracy of the test depends on the sample collection process. Improper sample collection, improper sample storage, or repeated freezing and thawing of the sample will affect the test result.

4. The test result of this reagent are for clinical reference only, a confirmed diagnosis should only be made after all clinical and laboratory findings have been evaluated.

5. Limited by the method of antibody detection reagents, for negative test results, it is recommended to use nucleic acid detection or virus culture identification methods for review and confirmation.

6. Positive test results do not rule out co-infections with other pathogens. A negative result of this reagent can be caused by:1) Improper sample collection, improper sample transfer or

handing, the virus titer in the sample is too low; 2) The level of SARS-CoV-2 antibodies is below the detection limit

of the test.3) Variations in viral genes may cause changes in antibody

determinants.

PERFORMANCE CHARACTERISTICS

A. Sensitivity and Specificity 596 clinical case samples which include 361 confirmed case samples* and 235 confirmed excluded case samples*, were obtained for testing, and then compared the test results between Wondfo SARS-CoV-2 Antibody Test (Lateral Flow Method) and the confirmed case samples. The results of sensitivity and specificity between the two method are show below.

* Confirmed cases were the patients diagnosed according to the treatment plan.

* Confirmed excluded cares were identified by negative PCR results.

Results analysis：Sensitivity: 86.43% (95%CI: 82.41%~89.58%) Specificity: 99.57% (95%CI: 97.63%~99.92%)Total consistent: 91.61% (95%CI: 89.10%~93.58%)

B. Cross-reactivitySpecimens which tested positive with following various agents from patients were investigated with Wondfo SARS-CoV-2 Antibody Test (Lateral Flow Method). The results showed no cross reactivity.

ReagentsClinical cases

Confirmed case samples

312

49

361

Total

313

283

596

Excluded case samples

1

234

235Total

Wondfo SARS-CoV-2 Antibody Test (Lateral Flow Method)

Positive

Negative

Parainfluenza virus antibodyInfluenza A antibodyInfluenza B antibodyChlamydia pneumonia antibody Mycoplasma pneumoniae antibody Adenovirus antibodyRespiratory syncytial virus antibodyHepatitis B surface antibodyHepatitis C virus antibodyTreponema pallidum antibodyHIV antibodyEB virus antibodyMeasles virus antibodyCytomegalovirus antibodyEnterovirus type 71 antibodyMumps antibodyVaricella-zoster virus positive sample

LIMITATIONS OF PROCEDURE

1. This reagent is designed to detect antibodies against SARS-CoV-2 in human whole blood, plasma, serum sample.

2. This reagent is a qualitative assay. It is not designed to determine the quantitative concentration of SARS-CoV-2 antibodies.

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C. Interferences The test result of Wondfo SARS-CoV-2 Antibody Test (Lateral Flow Method) do not be interfered with the substance at the following concentration:

D. Precision1. Within run precision was determined by using 10 replicates of three

different specimens containing different concentrations of antibody.

SubstanceBilirubinHemoglobinTriglycerideRheumatoid factors Antinuclear antibody (ANA) titer Anti-mitochondrial antibody (AMA)Mouse IgG

Concentration250 μmol/L9 g/L15 mmol/L80 IU/mL1:24080 U/mL1000 μg/mL

The negative and positive values were correctly identified 100% of the time.

2. Between run precision was determined by using the three different specimens containing different concentrations of antibody in 3 different lots of test devices. Again negative and positive results were correctly identified 100% of the time.

BIBLIOGRAPHY

[1] Na Zhu, Ph.D., Dingyu Zhang, M.D., Wenling Wang, Ph.D., et al. (2020). A Novel Coronavirus from Patients with Pneumonia in China, 2019. The New England Journal of Medicine.

[2] Chen Wang, Peter W Horby, Frederick G Hayden, George F Gao. (2020). A novel coronavirus outbreak of global health concern. The Lancet, 395(10223), 470-473.

[3] Chaolin Huang, Yeming, et al. (2020). Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. The Lancet, 395(10223), 497-506.

[4] Nanshan Chen, Min Zhou, Xuan Dong, et al. (2020). Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: a descriptive study. The Lancet, 395(10223), 507-513.

[5] World Health Organization: Clinical management of severe acute respiratory infection when Novel coronavirus (nCoV) infection is suspected: Interim Guidance. 12 January, 2020.

INDEX OF SYMBOL

In VitroDiagnostic Use

Tests per Kit

Batch Number

See Instruction for Use

Manufacturing Date

Expiry Date

Keep Dry

Keep away from Sunlight

Do not reuse Catalog #Store between 2～30ºC2

Manufacturer


539-CGAFA INTEGRALINTEGRAL GOGGLE

DescripciónDescription

La gafa integral Climax 539 C ha sido diseñada para ofrecer una efectiva protección contra el riesgo de impacto de partículas de alta velocidad y baja energía y frente a salpicaduras y particulas de polvo gruesas y finas. Por su especial diseño posee un gran campo visual y puede ser usada con gafas graduadas.

Climax 539 C integral goggles have been designed to offer effective protection against the impact of high speed, splashes and low energy particles and large and fine dust particles.. Thanks to their special design, they offer a view field of vision and can be used whilr wearing corrective glasses.

Características

MarcadoMarking

CharacteristicsMonturaLa montura está fabricada por inyección de PVC flexible y presenta en todo su perímetro interior una ranura para el alojamiento ocular y los resaltes necesarios para su fijación. Sin ventilación.

FrameThe frame is manufactured in injected �exible PVCand It has a groove on its inside surface to hold theeyepiece and the necessary projection to secure itin position. No ventilation.

OcularesSon de forma panorámica (en una sola pieza), planos, incoloros, y con un espesor nominal de 1.15 mm.

LensesThey are panoramic (in one piece). They are eatand colourless with a nominal thickness of1.15 mm.

RecambiosOcular de repuesto, fácilmente recambiable encajandomediante presión a la montura.

Spare partsSpace lens, easily changed by press �tting intothe frame.

TratamientoAntiempañanteAntirayaduras

TreatmentAnti-fogAnti-scratch

Protección contra electricidad estática Protection against static electricity

Para uso en atmósferas potencialmente explosivas (ATEX)

To use in potentially explosive atmospheres. (ATEX)

Marcado del ocularLens marking

Marcado monturaFrame marking

1FN

PCX EN 166 345F

MADE IN SPAIN



Infrared Non-Contact Temple Thermometer

Model: HA500

Clinically Accurate

This Temple thermometer has been clinically tested in several big

teaching hospitals based on the protocol of ASTM E1965-98:2009

regulatory standard, covering sufficient febrile and normal body

temperature subjects with satisfied clinical repeatabil ity and

measuring accuracy comparing to the concurrent oral temperature

measurement reading.

Patent Nos : ZL 2011 3 0359484.6

ASTM E1965-98:2009Temple Thermometer

Non Contact

Storage Case

• Measurement distance within 5cm (2 inch)

• 1 second measurement

• Temple Temperature

• Object temperature

• Fever alarm

• 9 memories

• °C / °F switchable

• Backlight

• Auto shut-off

• Low battery indicator

• Self-diagnosis for malfunction

Model Qty per carton Carton volume

HA500 50 pcs 0.072 cbm/ctn

Storage and Transportation Condition

-25°C~55°C(-13°F~131°F)

≦95% RH, 700~1060 hPa



NEGATIVE PRESSUREISOLATION CHAMBER

Equipment for transporting an infected patient requiring en route monitoring.

This isolation chamber is at negative pressure with respect to the surrounding area to prevent

pathogenic microorganisms from escaping. Negative pressure is maintained by a filter motor

attached to the feet end.


NEGATIVE PRESSUREISOLATION CHAMBER

The chamber was designed with simplicity and reliability in mind. Its compact size makes it

easy to transport.

Features3 alarms: Audio, Visual, Vibration to indicate filter blockage and low battery.

It is maintained at a constant level to ensure optimal comfort for the user.

The user retains their mobility and feels less fatigue than with simple breathing apparatus.

Dimensions: 15x85x100mm

Weight: 1350g

Suction capacity: 150-200l/min

Battery: NiMH-6-Pack 7.2V 4300mAh

Battery Life: 8H

Charge Time: +-6H

Applied standards： P.P.E Directive (category 3).

EN 421-1994, EN 374-1-2003, EN 388-2003


EJ120 Air Purifier

■ Meet EJ, the Tesla of air purifiers - made in USA with a super efficient & quiet German

motor and top notch performance. Energy Star.

■ CNN Best Air Purifier for Large Homes 2019. Women's Health Editor's Choice 2019

■ Removes Allergies, Asthma, Dust, Bacteria, Pollen, Mold Spores, Pet Dander, Smoke

■ Medical Grade HEPA filter (MERV17) tested to remove 99.99% of airborne allergens &

particulates. Ideal for tobacco smoke removal

■ See how it compares to air purifiers that "destroy" pollutants

■ What's included: Air purifier with filters installed, User's Manual

■ If you are in a high dust environment we suggest adding the pre-filter in front of the

carbon filter


EJ120 Air Purifier

Meet the EJ120 Air Purifier

EJ is the newer, smaller version of the ERIK650A. EJ stands for Erik Junior.

While it is smaller, the EJ120 has a strong CADR of 360 for pollen and is our quietest

high performance air purifier. And it does this with only drawing 52 watts of power.

We searched the world to build the ultimate air purifiers. In Germany we found the l

argest factory of high performance motors, just like a Tesla engine. So, you get high

performance and reliability with low energy usage.

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Instruments & Equipment

Beijing Kanggaote Instruments and Equipments Co.LtdAdd:Floor 8,Tower 2,HANWEI International Phase 4, No. 186 Nansihuan West Road, Fengtai District, Beij ing, ChinaTel:86-010-68940148Fax:86-010-60862912Email: [email protected]:0086-13810851425

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