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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 3.5 AKTIV — 4 UDI-DI variants, MDR (Norgesplaster AS)

MD Atlas
Norgesplaster AS

Data from EUDAMED, last updated May 30, 2026

TF 3.5 AKTIV

7022750035005X

4 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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 7022750035005X
Device name: TF 3.5 AKTIV
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

4 UDI-DI variants

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Applied filters

basicUdiUlid01GQQ32HYA970APDQSQCN1BQRP

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

404207022750040429
404507022750040450
404907022750040498
404107022750040412