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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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Gehhilfe — 20 UDI-DI variants, MDR (CareLiv Produkte OHG)

MD Atlas
CareLiv Produkte OHG

Data from EUDAMED, last updated May 23, 2026

Gehhilfe

PP02014GEHHI03

20 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: CareLiv Produkte OHG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: PP02014GEHHI03
Device name: Gehhilfe
Issuing agency: IFA
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 30, 2025

Manufacturer & authorised representative

Manufacturer

Name: CareLiv Produkte OHG
SRN: DE-MF-000040071
Country: Germany
Email: info@careliv.de
Phone: +493434140139

Variants by status

UDI-DI variants

20 UDI-DI variants

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Applied filters

basicUdiUlid01K6CR8RKT8G9CB97VW2BWDA7F

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

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