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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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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

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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

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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

T66380201000C9004035459213226
T66328100600C9004035459221436
T66378200600C9004035459191296
T66380200800C2004035459213097
T66370101300C8004035459178440
T66360100700B2104035459063524
T66390101000C8004035459186919
T66360100500B8204035459175098
T66368200500B2104035459192576
T66370100100B8004035459178235
T66360101000C2104035459063630
T66370100200B8004035459178242
T66360100700A2104035459063425