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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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F1 — 4 UDI-DI variants, MDR (Berollka-aktiv Rollstuhltechnik GmbH)

MD Atlas
Berollka-aktiv Rollstuhltechnik GmbH

Data from EUDAMED, last updated May 23, 2026

F1

40663582050U7000000UB

4 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: Berollka-aktiv Rollstuhltechnik GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 40663582050U7000000UB
Device name: F1
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 15, 2023

Manufacturer & authorised representative

Manufacturer

Name: Berollka-aktiv Rollstuhltechnik GmbH
SRN: DE-MF-000007043
Country: Germany
Email: info@berollka.de
Phone: +49 7261 73510

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GVJ0HRJWH5TSP5Z3B3SGVX8A

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

U70004066358200000
U70104066358200017
U70204066358200024
U70304066358200031