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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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Innova 1.0 — 5 UDI-DI variants, MDR (vivipar GmbH)

MD Atlas
vivipar GmbH

Data from EUDAMED, last updated May 23, 2026

Innova 1.0

42700022467BettenEM

5 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

Active device

Identity & classification

Basic UDI-DI: 42700022467BettenEM
Device name: Innova 1.0
Device model: Entbindungsbetten
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

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JQBQZ122E7130QGDDQGQZB4Y

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

21.20.00004270002246713
21.00.00004270002246720
22.00.00004270002246706
20.00.00004270002246737
25.00.00004270002246744