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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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APARENT® Aktiv — 2 UDI-DI variants, MDR (Albosan AG)

MD Atlas
Albosan AG

Data from EUDAMED, last updated May 23, 2026

APARENT® Aktiv

426074063Arm-Lagerung53

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: Albosan AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426074063Arm-Lagerung53
Device name: APARENT® Aktiv
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 5, 2026

Manufacturer & authorised representative

Manufacturer

Name: Albosan AG
SRN: CH-MF-000020071
Country: Switzerland
Email: info@albosan.ch

Authorised representative

Name: BEO MedConsulting Berlin GmbH
SRN: DE-AR-000006764
Country: Germany
Phone: +49(0)3031804530

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KJZ7D3KTKHTDDEXGEY1KVZ5D

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

10.00104260740630004
10.00204260740630011