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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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ORTHESE ABDUCTION DE L'EPAULE — 2 UDI-DI variants, MDR (ORTHOMEDICA)

MD Atlas
ORTHOMEDICA

Data from EUDAMED, last updated May 23, 2026

ORTHESE ABDUCTION DE L'EPAULE

3665012ABDUCTIONZ2

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: ORTHOMEDICA

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 3665012ABDUCTIONZ2
Device name: —
Device model: ORTHESE ABDUCTION DE L'EPAULE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: ORTHOMEDICA
SRN: FR-MF-000001811
Country: France
Email: marie.regaldi@orthomedica.fr
Phone: 03 80 68 85 30

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS2Q5SJKZE7N8H0V3D5W57YG

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

Coussin abduction de l'épaule L03665012001970
Coussin abduction de l'épaule S03665012001963