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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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BU00078 — 23 UDI-DI variants, MDR (Össur Iceland ehf.)

MD Atlas
Össur Iceland ehf.

Data from EUDAMED, last updated May 31, 2026

BU00078

5690967BU00078NW

23 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: 5690967BU00078NW
Device name: —
Device model: BU00078
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 27, 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

23 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSN09CKVG97Q42VEGDR947EB

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

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L-54464005690977438521
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L-54451205690977438439
L-54462105690977438514
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L-54462005690977438507
L-54464105690977438538
L-54454105690977438460
L-54461305690977438491
L-54451305690977438446
L-54461105690977438477
L-54451105690977438422
L-55100205690967541620
L-55200005690967490454
L-64100005690967118358
L-64110005690967135898
UTF0001-CPI05690977249097
UTF000105690977404953
UTT0001-CPI05690977249103
UTT000105690967585372
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