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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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lipivir(R) — 4 UDI-DI variants, MDR (Devirex AG)

MD Atlas
Devirex AG

Data from EUDAMED, last updated May 23, 2026

lipivir(R)

7649994728lipivir0001CG

4 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: Devirex AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 7649994728lipivir0001CG
Device name: lipivir(R)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 21, 2022

Manufacturer & authorised representative

Manufacturer

Name: Devirex AG
SRN: CH-MF-000017711
Country: Switzerland
Email: info@devirex.ch
Phone: +41 41 758 00 00

Authorised representative

Name: Stefan Gangkofner
SRN: DE-AR-000005777
Country: Germany

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01FWDQW2PRH2VBQRYX4PZ2FG6W

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

lipivir07629999031685
lipivir(R)07629999031678
lipivir(R)07649994728113
lipivir(R)07649994728014