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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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BU00001 — 266 UDI-DI variants, MDR (Össur Iceland ehf.)

MD Atlas
Össur Iceland ehf.

Data from EUDAMED, last updated May 31, 2026

BU00001

5690967BU00001MT

266 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: 5690967BU00001MT
Device name: —
Device model: BU00001
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 26, 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

266 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSJ5S1KZZKKVNPVBDMZWP9G0

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

I-TF6733805690967513252
I-TF6732805690967513207
I-TF6734005690967513269
I-TF6733605690967513245
I-TF6735005690967513283
I-TF6732505690967513184
I-TF6732605690967513191
I-TF6783605690967513375
I-TF6783405690967513368
I-TF6782505690967513313
I-TF6783005690967513344
I-TF6733005690967513214
I-TF6733405690967513238
I-TF6733205690967513221
I-TF6783205690967513351
I-TF6783805690967513382