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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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N!ce — 64 UDI-DI variants, MDR (Institut Straumann AG)

MD Atlas
Institut Straumann AG

Data from EUDAMED, last updated May 23, 2026

N!ce

0763003170001Q4

64 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: 0763003170001Q4
Device name: N!ce
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 13, 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

64 UDI-DI variants

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Applied filters

basicUdiUlid01KKKPRN8E2WBH5TG87CB98GWE

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

010.715907630031735119
010.710907630031734624
010.715507630031735072
010.706307630031738660
010.714407630031734976
010.711307630031734662
010.713507630031734884
010.715207630031735058
010.714007630031734938
010.706507630031738684
010.705707630031731067
010.701307630031704429
010.711407630031734679
010.714907630031735027

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