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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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Attelle de Pouce — 9 UDI-DI variants, MDR (MEDISPORT)

MD Atlas
MEDISPORT

Data from EUDAMED, last updated May 19, 2026

Attelle de Pouce

3664617PGT20XZ

9 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: MEDISPORT

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3664617PGT20XZ
Device name: Attelle de Pouce
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 16, 2025

Manufacturer & authorised representative

Manufacturer

Name: MEDISPORT
SRN: FR-MF-000000677
Country: France
Email: medifab@medisport.fr

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01K59BDME1XH6JDP6RN6ZK3ZFG

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

Attelle de Pouce03664617003655
Attelle de Pouce03664617003648
Attelle de Pouce03664617003662
ATTELLE DE POUCE BILATERALE03664617006045
ATTELLE DE POUCE BILATERALE03664617006052
ATTELLE DE POUCE BILATERALE03664617006038
ATTELLE POUCE PREMIUM - GAMME EVOLUPHARM03664617008209
ATTELLE POUCE PREMIUM - GAMME EVOLUPHARM03664617008216
ATTELLE POUCE PREMIUM -GAMME EVOLUPHARM03664617008193