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 Coping: Variobase Coping — 10 UDI-DI variants, MDR

MD Atlas
Institut Straumann AG

Data from EUDAMED, last updated May 23, 2026

Final Coping: Variobase Coping

0763003170098RD

10 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0763003170098RD
Device name: Final Coping: Variobase Coping
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 24, 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

10 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

basicUdiUlid01KMFGGZ77F9T1XHSRS42WJW1J

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

010.542307630031773753
010.542207630031773746
023.004007630031773432
023.002707630031737175
023.002807630031737182
023.004107630031773449
010.608807630031737144
010.542007630031773722
023.003807630031773418
010.608707630031737137