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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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V-DENUPET — 9 UDI-DI variants, MDR (VITROMED GmbH)

MD Atlas
VITROMED GmbH

Data from EUDAMED, last updated May 23, 2026

V-DENUPET

426053179VDENUPET3Q

9 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: VITROMED GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426053179VDENUPET3Q
Device name: V-DENUPET
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Aug 13, 2025

Manufacturer & authorised representative

Manufacturer

Name: VITROMED GmbH
SRN: DE-MF-000005131
Country: Germany
Email: info@vitromed.com

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01K2H12JJWTT23MGP5XHR0EKZ4

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

V-DENUPET04260531790054
V-DENUPET04260531790092
V-DENUPET04260531790030
V-DENUPET04260531790085
V-DENUPET04260531790016
V-DENUPET04260531790061
V-DENUPET04260531790078
V-DENUPET04260531790009
V-DENUPET04260531790023