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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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MOBIDERM — 8 UDI-DI variants, MDR (THUASNE)

MD Atlas
THUASNE

Data from EUDAMED, last updated May 19, 2026

MOBIDERM

311179FR0019AEW

8 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

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 311179FR0019AEW
Device name: MOBIDERM
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 17, 2025

Manufacturer & authorised representative

Manufacturer

Name: THUASNE
SRN: FR-MF-000001201
Country: France
Email: service.conseil@thuasne.fr
Phone: +33 4 77 81 40 40

Variants by status

UDI-DI variants

8 UDI-DI variants

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Applied filters

basicUdiUlid01JXZX0615RKM7KABY4Z0A6KEQ

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

3710010250250103111790242437
3720010103000203111790242475
3710010331000203111790242451
3710010180250203111790874386
3710010331000103111790242444
3710010210250203111790874393
3720020103000203111790874379
3720010103000103111790242468