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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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Temporary Abutment, Sterile — 12 UDI-DI variants, MDR

MD Atlas
Institut Straumann AG

Data from EUDAMED, last updated May 23, 2026

Temporary Abutment, Sterile

0763003170101Q9

12 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

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Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 0763003170101Q9
Device name: Temporary Abutment, Sterile
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

12 UDI-DI variants

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Applied filters

basicUdiUlid01KKC07QNQATK5N7B3637ZBEVZ

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

022.0120S07630031753205
064.4324S07630031753236
064.4333S07630031753250
022.0117S07630031753175
064.4334S07630031753267
022.0118S07630031753182
064.4322S07630031753212
022.0119S07630031753199
022.0116S07630031753168
064.4332S07630031753243
064.4323S07630031753229
022.0115S07630031753151