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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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ProLift Argo — 2 UDI-DI variants, MDR (novacare gmbh)

MD Atlas
novacare gmbh

Data from EUDAMED, last updated May 23, 2026

ProLift Argo

42504796V080503995D

2 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: novacare gmbh

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 42504796V080503995D
Device name: ProLift Argo
Device model: ProLift
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 27, 2022

Manufacturer & authorised representative

Manufacturer

Name: novacare gmbh
SRN: DE-MF-000007623
Country: Germany
Email: info@novacare.de
Phone: +49632295650

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01G1NAWQKND1DKS71AJAZFK2RC

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

96021504250479624030
96021604250479624047