eudamed_udi Primary ID: 03664617005413

GENOUILLERE DE MAINTIEN MDS (UDI 03664617005413)

Manufactured by MEDISPORT

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The GENOUILLERE DE MAINTIEN MDS (Model/Catalog Number: 894.050) is a medical device manufactured by MEDISPORT. This product is indexed under FDA Product Code / Category Classification Y061209 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 894.050
Product Code / EMDN: Y061209
Device Name: Genouillère de Maintien
Database Sync Date: 2026-08-09 16:28:47

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of GENOUILLERE DE MAINTIEN MDS?

The registered manufacturer of record for GENOUILLERE DE MAINTIEN MDS is MEDISPORT.

What is the Primary UDI-DI identifier for GENOUILLERE DE MAINTIEN MDS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03664617005413.

What classification code is assigned to this device?

This device is registered under product classification code Y061209.

Similar Classification Devices (Y061209)

Other Devices by MEDISPORT

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