Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

BU00051 — 2,245 UDI-DI variants, MDR (Össur Iceland ehf.)

MD Atlas
Össur Iceland ehf.

Data from EUDAMED, last updated May 31, 2026

BU00051

5690967BU00051NA

2,245 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.

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5690967BU00051NA
Device name: —
Device model: BU00051
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

2,245 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KSN0900MAW7Q6D9HFG2XXCBS

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

SSPU925005690977368736
SHPE522005690977337039
SSPE4240LBR05690967850555
SSPE6240RBR05690967851293
SHPE728005690977337459
SSPE7290LBR05690967851712
SSPE7290L05690967851705
SHPE829205690977337602
SSPE3240R05690967850203
SSPE9270LBR05690967852115
SSPE6300RBR05690967851538
SSPU427005690977368392
SSPE1260LBR05690967849795
SSPE1240RBR05690967849733
SSPE1270L05690967849825
SSPE423005690977337978
SSPE826005690977338302
SHPE825005690977337510
SSPE4250RBR05690967850616
SSPE6230R05690967851248
SSPE927005690977338371
SSPE2250LBR05690967849993
SSPE830005690977338340
SSPE5230RBR05690967850890
SSPE3230LBR05690967850159