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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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BU00092 — 12 UDI-DI variants, MDR (Össur Iceland ehf.)

MD Atlas
Össur Iceland ehf.

Data from EUDAMED, last updated May 31, 2026

BU00092

5690967BU00092NQ

12 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: Össur Iceland ehf.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5690967BU00092NQ
Device name: —
Device model: BU00092
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: Össur Iceland ehf.
SRN: IS-MF-000000173
Country: Iceland
Email: info-europe@ossur.com
Phone: +31 (0) 499 462 840

Variants by status

UDI-DI variants

12 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KST1TN0SR167YGZ4Y80WJZR3

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

980121RB05690977437487
1088205690977132061
B-50210010105690977326286
WKSG-1BLK05690977188228
FOA00030205690967970406
FOA00040605690967970468
FOA00030105690967970390
FOA00040505690967970451
FOA00040405690967970444
FOA00040205690967970420
FOA00040105690967970413
FOA00040305690967970437