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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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Greifzange Falke — 6 UDI-DI variants, MDR (Rehastage GmbH)

MD Atlas
Rehastage GmbH

Data from EUDAMED, last updated May 23, 2026

Greifzange Falke

426063581FALKE5D

6 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: Rehastage GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426063581FALKE5D
Device name: Greifzange Falke
Device model: Greifzange Falke
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 14, 2021

Manufacturer & authorised representative

Manufacturer

Name: Rehastage GmbH
SRN: DE-MF-000009450
Country: Germany
Email: info@rehastage.de

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01FHQGZRS2NQ77BTQQB2KP1VA9

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

FALKE06004260635810092
FALKE07804260635810108
FALKE060L04260635810207
FALKE078L04260635810214
FALKE060P04260635810191
FALKE078P04260635810184