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

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Digital Impression — 12 UDI-DI variants, MDR (Institut Straumann AG)

MD Atlas
Institut Straumann AG

Data from EUDAMED, last updated May 23, 2026

Digital Impression

0763003170011Q7

12 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

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0763003170011Q7
Device name: Digital Impression
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 22, 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

12 UDI-DI variants

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Applied filters

basicUdiUlid01KPTE3DEVSJVJ2GBW45QKWZZT

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

025.000007630031710925
048.16807630031723246
065.003507630031738301
048.17307630031723284
025.002507630031728784
025.291507630031711854
032.04107630031729583
036.322007630031746764
025.491507630031712646
025.000107630031710932
048.16907630031723253
065.003807630031749024