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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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CONVERTER — 2 UDI-DI variants, MDR (THALES AVS FRANCE SAS)

MD Atlas
THALES AVS FRANCE SAS

Data from EUDAMED, last updated May 19, 2026

CONVERTER

37014401072H

2 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: THALES AVS FRANCE SAS

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 37014401072H
Device name: CONVERTER
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 15, 2022

Manufacturer & authorised representative

Manufacturer

Name: THALES AVS FRANCE SAS
SRN: FR-MF-000012704
Country: France
Email: Akim.Douchement.PRRC@thalesgroup.com
Phone: +33 6 72 97 00 96

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GMB28H3THTFKSRKDP5ERBQBZ

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

CONVERTER 5G03701440100295
CONVERTER 263003701440100318