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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 Poignet Main Flexion — 6 UDI-DI variants, MDR (MEDISPORT)

MD Atlas
MEDISPORT

Data from EUDAMED, last updated May 19, 2026

Attelle de Poignet Main Flexion

3664617PGT04Y3

6 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: 3664617PGT04Y3
Device name: Attelle de Poignet Main Flexion
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

6 UDI-DI variants

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Applied filters

basicUdiUlid01K59BK3WZR5AQ0Y1GE0EX5QYD

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 POIGNET MP EN FLEXION03664617008285
ATTELLE DE POIGNET MP EN FLEXION03664617008377
ATTELLE DE POIGNET MP EN FLEXION03664617008261
ATTELLE DE POIGNET MP EN FLEXION03664617008278
ATTELLE DE POIGNET MP EN FLEXION03664617008254
ATTELLE DE POIGNET MP EN FLEXION03664617008360