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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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TF 1.12 Urifix — 3 UDI-DI variants, MDR (Norgesplaster AS)

MD Atlas
Norgesplaster AS

Data from EUDAMED, last updated May 30, 2026

TF 1.12 Urifix

7022750011200QL

3 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: Norgesplaster AS

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Device characteristics

Administers medicine

Identity & classification

Basic UDI-DI: 7022750011200QL
Device name: TF 1.12 Urifix
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: Norgesplaster AS
SRN: NO-MF-000022061
Country: Norway
Email: post@norgesplaster.no
Phone: +4738152200

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G1TH1QZ0ETTX62NBMX632ZPJ

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

1210707034950121075
1218507034950121853
1226107034950122607