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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™ Final Prosthetic… — 2 UDI-DI variants, MDR

MD Atlas
InfinetaMed AG

Data from EUDAMED, last updated May 23, 2026

NUVENTUS NV.C™ Final Prosthetic Components

764046272FAUD

2 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: InfinetaMed AG

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Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 764046272FAUD
Device name: NUVENTUS NV.C™ Final Prosthetic Components
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Mar 17, 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

2 UDI-DI variants

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Applied filters

basicUdiUlid01KKY1B1SJA4PNJ67AYNF8GD11

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

174.110007640462721094
174.020007640462721087