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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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Gebärsaalwannen — 2 UDI-DI variants, MDR (vivipar GmbH)

MD Atlas
vivipar GmbH

Data from EUDAMED, last updated May 23, 2026

Gebärsaalwannen

42700022467WannenKJ

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: vivipar GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42700022467WannenKJ
Device name: —
Device model: Gebärsaalwannen
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 27, 2025

Manufacturer & authorised representative

Manufacturer

Name: vivipar GmbH
SRN: DE-MF-000008098
Country: Germany
Email: info@vivipar.de

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JQBR3DX9307Y1YVHAF7KWKM0

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

10.10.00004270002246768
10.00.00004270002246751