dental card-e rev.09-13 - eng
DESCRIPTION
Dental Card-e Rev.09-13 - EnGTRANSCRIPT
DentalCertificate
of Originalityand Care
Card
Patient’s name
Address
Telephone
Date
Stamp of dental clinic
Description of prosthetic-implant treatment and rehabilitation
18 17 16 15 14 13 12 11
48 47 46 45 44 43 42 41
Implant position
Description of prosthetic-implant treatment and rehabilitation
18 17 16 15 14 13 12 11 21 22 23 24 25 26 27 28
48 47 46 45 44 43 42 41 31 32 33 34 35 36 37 38
UR UL
LR LL
IMPLANT TYPEDiam / Length
POSITION
DATE OF IMPLANT
DATE OF RE-OPENING
TRANSMUCOUS SCREW
DATE OF PROSTHESIS
NOTES
Code of ABUTMENT, ATTACHMENT, OTHER
Apply the adhesive label present inside the package
IMPLANT TYPEDiam / Length
POSITION
DATE OF IMPLANT
DATE OF RE-OPENING
TRANSMUCOUS SCREW
DATE OF PROSTHESIS
NOTES
Code of ABUTMENT, ATTACHMENT, OTHER
Apply the adhesive label present inside the package Apply the adhesive label present inside the package
IMPLANT TYPEDiam / Length
POSITION
DATE OF IMPLANT
DATE OF RE-OPENING
TRANSMUCOUS SCREW
DATE OF PROSTHESIS
NOTES
Code of ABUTMENT, ATTACHMENT, OTHER
IMPLANT TYPEDiam / Length
POSITION
DATE OF IMPLANT
DATE OF RE-OPENING
TRANSMUCOUS SCREW
DATE OF PROSTHESIS
NOTES
Code of ABUTMENT, ATTACHMENT, OTHER
Apply the adhesive label present inside the package
IMPLANT TYPEDiam / Length
POSITION
DATE OF IMPLANT
DATE OF RE-OPENING
TRANSMUCOUS SCREW
DATE OF PROSTHESIS
NOTES
Code of ABUTMENT, ATTACHMENT, OTHER
Apply the adhesive label present inside the package Apply the adhesive label present inside the package
IMPLANT TYPEDiam / Length
POSITION
DATE OF IMPLANT
DATE OF RE-OPENING
TRANSMUCOUS SCREW
DATE OF PROSTHESIS
NOTES
Code of ABUTMENT, ATTACHMENT, OTHER
IMPLANT TYPEDiam / Length
POSITION
DATE OF IMPLANT
DATE OF RE-OPENING
TRANSMUCOUS SCREW
DATE OF PROSTHESIS
NOTES
Code of ABUTMENT, ATTACHMENT, OTHER
Apply the adhesive label present inside the package
IMPLANT TYPEDiam / Length
POSITION
DATE OF IMPLANT
DATE OF RE-OPENING
TRANSMUCOUS SCREW
DATE OF PROSTHESIS
NOTES
Code of ABUTMENT, ATTACHMENT, OTHER
Apply the adhesive label present inside the package Apply the adhesive label present inside the package
IMPLANT TYPEDiam / Length
POSITION
DATE OF IMPLANT
DATE OF RE-OPENING
TRANSMUCOUS SCREW
DATE OF PROSTHESIS
NOTES
Code of ABUTMENT, ATTACHMENT, OTHER
IMPLANT TYPEDiam / Length
POSITION
DATE OF IMPLANT
DATE OF RE-OPENING
TRANSMUCOUS SCREW
DATE OF PROSTHESIS
NOTES
Code of ABUTMENT, ATTACHMENT, OTHER
Apply the adhesive label present inside the package
IMPLANT TYPEDiam / Length
POSITION
DATE OF IMPLANT
DATE OF RE-OPENING
TRANSMUCOUS SCREW
DATE OF PROSTHESIS
NOTES
Code of ABUTMENT, ATTACHMENT, OTHER
Apply the adhesive label present inside the package Apply the adhesive label present inside the package
IMPLANT TYPEDiam / Length
POSITION
DATE OF IMPLANT
DATE OF RE-OPENING
TRANSMUCOUS SCREW
DATE OF PROSTHESIS
NOTES
Code of ABUTMENT, ATTACHMENT, OTHER
IMPLANT TYPEDiam / Length
POSITION
DATE OF IMPLANT
DATE OF RE-OPENING
TRANSMUCOUS SCREW
DATE OF PROSTHESIS
NOTES
Code of ABUTMENT, ATTACHMENT, OTHER
Apply the adhesive label present inside the package
IMPLANT TYPEDiam / Length
POSITION
DATE OF IMPLANT
DATE OF RE-OPENING
TRANSMUCOUS SCREW
DATE OF PROSTHESIS
NOTES
Code of ABUTMENT, ATTACHMENT, OTHER
Apply the adhesive label present inside the package Apply the adhesive label present inside the package
IMPLANT TYPEDiam / Length
POSITION
DATE OF IMPLANT
DATE OF RE-OPENING
TRANSMUCOUS SCREW
DATE OF PROSTHESIS
NOTES
Code of ABUTMENT, ATTACHMENT, OTHER
IMPLANT TYPEDiam / Length
POSITION
DATE OF IMPLANT
DATE OF RE-OPENING
TRANSMUCOUS SCREW
DATE OF PROSTHESIS
NOTES
Code of ABUTMENT, ATTACHMENT, OTHER
Apply the adhesive label present inside the package
IMPLANT TYPEDiam / Length
POSITION
DATE OF IMPLANT
DATE OF RE-OPENING
TRANSMUCOUS SCREW
DATE OF PROSTHESIS
NOTES
Code of ABUTMENT, ATTACHMENT, OTHER
Apply the adhesive label present inside the package Apply the adhesive label present inside the package
IMPLANT TYPEDiam / Length
POSITION
DATE OF IMPLANT
DATE OF RE-OPENING
TRANSMUCOUS SCREW
DATE OF PROSTHESIS
NOTES
Code of ABUTMENT, ATTACHMENT, OTHER
Follow-upDate Comments
Date Comments
Date Comments
Follow-upDate Comments
Date Comments
Date Comments
Follow-upDate Comments
Date Comments
Date Comments
Follow-upDate Comments
Date Comments
Date Comments
The Sweden & Martina dental implants are made of
“commercially pure” medical titanium because scientific
research has shown that this metal is absolutely biocompatible
with human tissues, which is a critical factor for determining
bone integration. The prosthetic components can also be made
of commercially pure medical titanium, with different degrees
of resistance, or zirconium, a ceramic compound used for its
special aesthetic characteristics and high wear resistance.
The company’s commitment in the search for the highest
quality raw materials, certificate of origin, allows your dentist
to always choose the best option for your clinical needs.
Materials
The duration of implant rehabilitation is subjective, but also
depends on the patient’s good oral hygiene. This is confirmed
during the follow-ups, which allow immediately evaluating
the onset of any peri-implantitis.
We recommend you always follow the directions and the pre-
and post-operative instructions of your implant expert and
contact him if you have doubts on how to clean and care for
your implant.
The Sweden & Martina dental implants are made of
“commercially pure” medical titanium because scientific
research has shown that this metal is absolutely biocompatible
with human tissues, which is a critical factor for determining
bone integration. The prosthetic components can also be made
of commercially pure medical titanium, with different degrees
of resistance, or zirconium, a ceramic compound used for its
special aesthetic characteristics and high wear resistance.
The company’s commitment in the search for the highest
quality raw materials, certificate of origin, allows your dentist
to always choose the best option for your clinical needs.
The duration of implant rehabilitation is subjective, but also
depends on the patient’s good oral hygiene. This is confirmed
during the follow-ups, which allow immediately evaluating
the onset of any peri-implantitis.
We recommend you always follow the directions and the pre-
and post-operative instructions of your implant expert and
contact him if you have doubts on how to clean and care for
your implant.
Care and Maintenance Instructions
Sweden & Martina has always actively supported the protocols
of experimental and clinical research conducted by leading
universities and private research centres. This synergy has led
to the publication of hundreds of scientific articles in important
national and international journals, which examined and
tested all the characterises of the Sweden & Martina implants,
from the surface treatments to the morphology, from the
implant-prosthesis connections to the use of these implants in
post-extraction and/or immediate load protocols.
The activities to support research, culture and ethics in the
field of dental implants is a reflection of the company’s
mission, whose products are evaluated and developed based
on valuable information provided by researchers and clinicians
aimed at offering patients the most advanced solutions in the
shortest times.
This Dental Card certifies that the implants and prosthetic
components used for your implant-supported prosthetic
solutions are original, that their quality and technology
complies with the UNI EN ISO 9001:2008 / UNI EN 13485:2012
standards and that they carry the CE 0476 marking in
accordance with European Directive No. 93/42 concerning
Medical Devices, adopted with Legislative Decree No. 46/1997
and Directive No. 47/2007, adopted with Legislative Decree
No. 37/2010.
This Dental Card will allow any dentist to recognise your
implant and intervene accordingly.
Certification of Quality
Sweden & Martina has always actively supported the protocols
of experimental and clinical research conducted by leading
universities and private research centres. This synergy has led
to the publication of hundreds of scientific articles in important
national and international journals, which examined and
tested all the characterises of the Sweden & Martina implants,
from the surface treatments to the morphology, from the
implant-prosthesis connections to the use of these implants in
post-extraction and/or immediate load protocols.
The activities to support research, culture and ethics in the
field of dental implants is a reflection of the company’s
mission, whose products are evaluated and developed based
on valuable information provided by researchers and clinicians
aimed at offering patients the most advanced solutions in the
shortest times.
Scientific Research
This Dental Card certifies that the implants and prosthetic
components used for your implant-supported prosthetic
solutions are original, that their quality and technology
complies with the UNI EN ISO 9001:2008 / UNI EN 13485:2012
standards and that they carry the CE 0476 marking in
accordance with European Directive No. 93/42 concerning
Medical Devices, adopted with Legislative Decree No. 46/1997
and Directive No. 47/2007, adopted with Legislative Decree
No. 37/2010.
This Dental Card will allow any dentist to recognise your
implant and intervene accordingly.
DEN
TAL
CA
RD
-E r
ev.0
9-13
Sweden & Martina S.p.A.Via Veneto, 1035020 Due Carrare (PD), ItalyTel. +39 049 91 24 300Fax +39 049 91 24 [email protected]
Sweden & Martina Mediterranea S.L.Sorolla Center, Oficina 504Av.da Cortes Valencianas 58, 5pl46015-Valencia, EspañaTel. [email protected] gratuito 900993963
www.sweden-martina.com
dental card-e