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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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Osstell Instrument — 3 UDI-DI variants, MDR (Osstell AB)

MD Atlas
Osstell AB

Data from EUDAMED, last updated May 30, 2026

Osstell Instrument

9010522Beacon1C5

3 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: Osstell AB

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 9010522Beacon1C5
Device name: Osstell Instrument
Device model: Osstell Beacon
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 11, 2026

Manufacturer & authorised representative

Manufacturer

Name: Osstell AB
SRN: SE-MF-000002162
Country: Sweden
Email: info@osstell.com

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRB56AFTQMEDD7AEY1MQ382Y

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

10066809010522002650
0808614809010522002636
10310009010522002674