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.

BU00008 — 27 UDI-DI variants, MDR (Össur Iceland ehf.)

MD Atlas
Össur Iceland ehf.

Data from EUDAMED, last updated May 31, 2026

BU00008

5690967BU00008N9

27 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?

UDI-DI variants

27 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

basicUdiUlid01KSJB7MBDJ4TDFHDF69K4G44Y

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-30000605690967075286
I-30002205690967075385
I-30000705690967075293
I-30002605690967075408
I-30002405690967075392
I-30001905690967075361
I-30001205690967075323
I-30001105690967075316
I-30002005690967075378
I-30001605690967075347
I-30001705690967075354
I-30001405690967075330
I-30000905690967075309
I-61036805690967084615
I-61038805690967084639
I-61037805690967084622
I-61033805690967084585
I-61039805690967084646
I-61035805690967084608
I-61034805690967084592
K-19010005690967077198
K-19010105690967106997
K-19011005690967107086
K-19010205690967107031
K-19015005690967165154

1 2

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5690967BU00008N9
Device name: —
Device model: BU00008
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