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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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GILET ORTHOPEDIQUE — 6 UDI-DI variants, MDR (DE FIL EN AIGUILLE)

MD Atlas
DE FIL EN AIGUILLE

Data from EUDAMED, last updated May 19, 2026

GILET ORTHOPEDIQUE

3760362060001VN

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: DE FIL EN AIGUILLE

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3760362060001VN
Device name: GILET ORTHOPEDIQUE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 22, 2022

Manufacturer & authorised representative

Manufacturer

Name: DE FIL EN AIGUILLE
SRN: FR-MF-000017404
Country: France
Email: contact@defil.fr
Phone: +3389755610

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01FT0MEGR2ZXYQF2WTJ61C7GE6

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

DEFIL37603620600311
DEFIL37603620600618
DEFIL37603620600519
DEFIL37603620600212
DEFIL37603620600113
DEFIL37603620600410