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.

CICATREX MASS KOPF NAT.G. — 111 UDI-DI variants, MDR

MD Atlas
Thuasne Deutschland GmbH

Data from EUDAMED, last updated May 23, 2026

CICATREX MASS KOPF NAT.G.

4035459DE1414A3V

111 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: Thuasne Deutschland GmbH

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: 4035459DE1414A3V
Device name: CICATREX MASS KOPF NAT.G.
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 22, 2025

Manufacturer & authorised representative

Manufacturer

Name: Thuasne Deutschland GmbH
SRN: DE-MF-000006210
Country: Germany
Email: ra@thuasne.de

Variants by status

UDI-DI variants

111 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

basicUdiUlid01KD2TR0ZWMW0CJS3HQ37K4H0M

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

34051240200311504035459335300
34051240204013804035459410045
34051240203912804035459409971
34051240200312504035459335324
34051240200212704035459335270
34051230202310504035459335133
34051240204011504035459335515
34051240200312604035459335331
34051240202313704035459401036
34051240203913404035459423434
34051240205013404035459423458
34051240203912004035459335454
34051240203913704035459401067
34051240200212804035459409940
34051240202310504035459335355
34051240204011004035459335508
34051240203913504035459401043
34051240203910504035459335423
34051230203910504035459335171
34051240200212004035459335249
34051240202313804035459410021
34051240205113404035459432719
34051240200213804035459410007
34051230200610504035459335096
34051240200213604035459400961

1 2 3 4 5