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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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Système NEOFOOT — 9 UDI-DI variants, MDR (NEOORTHOPEDIE)

MD Atlas
NEOORTHOPEDIE

Data from EUDAMED, last updated May 19, 2026

Système NEOFOOT

3770033655NEOFOO2023NFJW

9 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: NEOORTHOPEDIE

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3770033655NEOFOO2023NFJW
Device name: Système NEOFOOT
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 11, 2025

Manufacturer & authorised representative

Manufacturer

Name: NEOORTHOPEDIE
SRN: FR-MF-000038032
Country: France
Email: contact@neo-orthopedie.fr
Phone: 0442798925

Variants by status

UDI-DI variants

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KC6FAED6FMG2TGQBGM1Q2MNC

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

barre 2103770033655030
barre 2403770033655023
barre 2703770033655016
barre 3003770033655009
languette NEOFOOT03770033655047
NEOFOOT D4003770033655085
NEOFOOT D6003770033655078
NEOFOOT G4003770033655061
NEOFOOT G6003770033655054