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 — 2,121 UDI-DI variants, MDR (Össur Iceland ehf.)

MD Atlas
Össur Iceland ehf.

Data from EUDAMED, last updated May 31, 2026

BU00051

5690967BU00051NA

2,121 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

2,121 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

PXT0122LBR05690967800048
PXTU429RBR05690967803766
PXT0527L05690967801434
PXTU223LBR05690967802905
PXTU424L05690967803537
PXTU430RBR05690967803803
PXTU629L05690967804459
PXT0425LBR05690967801007
PXT0629RBR05690967801908
PXT0225RBR05690967800420
PXT0329RBR05690967800826
PXT0322LBR05690967800529
PXTU125L05690967802738
PXT0323L05690967800550
PXT0224L05690967800352
PXTU328R05690967803353
PXTU726RBR05690967804602
PXT0326R05690967800697
PXT0324R05690967800611
PXT0125R05690967800178
PXTU122L05690967802615
PXTU630R05690967804510
PXTU624R05690967804275
PXT0430RBR05690967801229
PXTU727LBR05690967804626