Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Final Abutment: Variobase — 200 UDI-DI variants, MDR

MD Atlas
Institut Straumann AG

Data from EUDAMED, last updated May 23, 2026

Final Abutment: Variobase

0763003170097RB

200 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Institut Straumann AG

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 0763003170097RB
Device name: Final Abutment: Variobase
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Mar 10, 2026

Manufacturer & authorised representative

Manufacturer

Name: Institut Straumann AG
SRN: CH-MF-000009933
Country: Switzerland
Email: info@straumann.com
Phone: +41 61 965 11 11

Authorised representative

Name: Etkon GmbH
SRN: DE-AR-000009335
Country: Germany
Phone: +49 89 30 90 75-0

Variants by status

UDI-DI variants

200 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KKBP84J5ZE6769FBVHYXNCWG

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

048.37807630031737205
048.71007630031725936
022.010807630031736253
062.502607630031771414
062.494507630031738981
037.220107630031746580
048.87807630031736086
010.542607630031773784
010.604507630031734389
010.605007630031734433
010.609907630031738936
062.497207630031740946
010.607807630031736345
022.010907630031736260
022.002107630031707741
062.493607630031740908
062.500907630031771247
010.542907630031773814
010.616507630031746191
010.616407630031746184
062.506007630031775184
010.616207630031746160
010.536607630031771070
010.607507630031736314
010.613307630031740588

1 2 3 4 5