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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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Recrea (elektrisch) — 2 UDI-DI variants, MDR (Greiner GmbH)

MD Atlas
Greiner GmbH

Data from EUDAMED, last updated May 23, 2026

Recrea (elektrisch)

406609847E8D

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: Greiner GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 406609847E8D
Device name: Recrea (elektrisch)
Device model: 477E
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 14, 2023

Manufacturer & authorised representative

Manufacturer

Name: Greiner GmbH
SRN: DE-MF-000007660
Country: Germany
Email: thomas.wegmann@greiner-gmbh.de
Phone: 07144/811241

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HHKXEFJAWTKPRJ8WZ7KX9116

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

964770404066098477021
477030004066098477052