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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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NUVENTUS NV.C™ Impression analog… — 3 UDI-DI variants, MDR

MD Atlas
InfinetaMed AG

Data from EUDAMED, last updated May 23, 2026

NUVENTUS NV.C™ Impression analog Components

764046272ANUQ

3 UDI-DI variants

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

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

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 764046272ANUQ
Device name: NUVENTUS NV.C™ Impression analog Components
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: InfinetaMed AG
SRN: CH-MF-000045034
Country: Switzerland
Email: RAQA@infinetamed.com

Authorised representative

Name: MedNet EC-REP IIb GmbH
SRN: DE-AR-000011192
Country: Germany

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KM0NB3KW99ATMC8S0QZJYJ6F

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

175.020007640462721193
181.351207640462721131
182.501207640462721179