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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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MAMILLEN ERGÄNZUNGSSET 8TEILIG — 10 UDI-DI variants, MDR

MD Atlas
Thuasne Deutschland GmbH

Data from EUDAMED, last updated May 23, 2026

MAMILLEN ERGÄNZUNGSSET 8TEILIG

4035459DE1202D3A

10 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: 4035459DE1202D3A
Device name: MAMILLEN ERGÄNZUNGSSET 8TEILIG
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

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KCRZ93DS686XWVP9SCD5D52B

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

T8312710910419904035459074094
T8312810920429904035459074131
T8312810920419904035459074179
T8312711210429904035459074070
T83125104035459073851
T8312811220419904035459074193
T8312711210419904035459074117
T8312811220429904035459074155
T83125204035459417204
T8312710910429904035459074056