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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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BU00049 — 365 UDI-DI variants, MDR (Össur Iceland ehf.)

MD Atlas
Össur Iceland ehf.

Data from EUDAMED, last updated May 31, 2026

BU00049

5690967BU00049NP

365 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: 5690967BU00049NP
Device name: —
Device model: BU00049
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

365 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSN093Z4Z8536TE0R5YR5X15

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

K2PU428R05690977400139
K2PU428L05690977400115
K2PU226LBR05690977400528
K2PU527R05690977400252
K2PU122R05690977399914
K2P0121R05690977380608
K2P0124LBR05690977380714
K2P0327LBR05690977381155
K2P0228LBR05690977381032
K2PU526R05690977400214
K2PU021L05690977399693
K2P0223RBR05690977380851
K2P0428RBR05690977381377
K2PU325R05690977400658
K2PU228LBR05690977400603