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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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ak 5010 MBS — 2 UDI-DI variants, MDR (AKRUS GmbH & Co. KG)

MD Atlas
AKRUS GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

ak 5010 MBS

426064794ak5010MBSEU

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: AKRUS GmbH & Co. KG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426064794ak5010MBSEU
Device name: ak 5010 MBS
Device model: Examination chair
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 14, 2025

Manufacturer & authorised representative

Manufacturer

Name: AKRUS GmbH & Co. KG
SRN: DE-MF-000005262
Country: Germany
Email: info@akrus.de
Phone: +49 4121 791930

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K7GTCZD4HA2XXD3DFB3F90Z3

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

277.00000004260647941524
277.00000704260647941555