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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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Genouillère Articulée — 6 UDI-DI variants, MDR (MEDISPORT)

MD Atlas
MEDISPORT

Data from EUDAMED, last updated May 19, 2026

Genouillère Articulée

3664617GEN13TM

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: 3664617GEN13TM
Device name: Genouillère Articulée
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

basicUdiUlid01K58YHCFRCGBT508VABE3HARF

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 GENOU ARTICULEE OPEN03664617008100
ATTELLE DE GENOU ARTICULEE OPEN03664617008155
ATTELLE DE GENOU ARTICULEE OPEN03664617008124
ATTELLE DE GENOU ARTICULEE OPEN03664617008117
ATTELLE DE GENOU ARTICULEE OPEN03664617008148
ATTELLE DE GENOU ARTICULEE OPEN03664617008131