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.

HAFTPAD FÜR SILIMA® XTRA — 663 UDI-DI variants, MDR

MD Atlas
Thuasne Deutschland GmbH

Data from EUDAMED, last updated May 23, 2026

HAFTPAD FÜR SILIMA® XTRA

4035459DE1202A34

663 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: 4035459DE1202A34
Device name: HAFTPAD FÜR SILIMA® XTRA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 18, 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

663 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

basicUdiUlid01KCRWK3SJDTT4H4X2AZDJEZDZ

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

T66360100200A2204035459063081
T66374100600B2004035459125765
T66380200900C2004035459213158
T66368200700B8204035459192965
T66390100600B8004035459186810
T66360100600C8204035459175180
T66370101000C9004035459178648
T66380200700B9004035459213028
T66378201200C8004035459191128
T66360100700A9104035459175913
T66328100100B8004035459221214
T66360100200A9204035459175562
T66328100500B8004035459221337
T66378201100C2004035459190886
T66360100700C2104035459063609
T66380200800B2004035459213066
T66378201100B8004035459191029
T66374100300C9004035459179034
T66368200400A2104035459192330
T66380200600B9004035459212960
T66360100500C8204035459175173
T66368200900B2204035459193306
T66374100200B2004035459125727
T66360100500B8104035459175395
T66370100400C2004035459064736