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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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CERVI-MOLL — 14 UDI-DI variants, MDR (Thuasne Deutschland GmbH)

MD Atlas
Thuasne Deutschland GmbH

Data from EUDAMED, last updated May 23, 2026

CERVI-MOLL

4035459DE0102A2J

14 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: 4035459DE0102A2J
Device name: CERVI-MOLL
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 8, 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

14 UDI-DI variants

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Applied filters

basicUdiUlid01KBYMDAA99RB2R9HRXK9JQN92

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

T4919032051201304035459265232
T4919032031001604035459265065
T4919032021201604035459265003
T4919032040651604035459265102
T4919032021201304035459264990
T4919032050651604035459265188
T4919032031201304035459265072
T4919032040651304035459265096
T4919032041201604035459265164
T4919032041001304035459265133
T4919032050651304035459265171
T4919032051201604035459265249
T4919032031201604035459265089
T4919032021001304035459264976