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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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Organization name
UDI-DI code
Reference / catalog number

barre 21 — Class I MDR by NEOORTHOPEDIE

MD Atlas
NEOORTHOPEDIE

EUDAMED last updated this device on Dec 11, 2025

barre 21

3770033655NEOFOO2023NFJW

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: NEOORTHOPEDIE
UDI-DI code: 03770033655030
Reference / catalog number: NEO2023NFB21

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Manufacturer information

Organization name: NEOORTHOPEDIE
SRN: FR-MF-000038032
Manufacturer status: Active

Related devices

barre 243770033655NEOFOO2023NFJWOn the market barre 273770033655NEOFOO2023NFJWOn the market barre 303770033655NEOFOO2023NFJWOn the market languette NEOFOOT3770033655NEOFOO2023NFJWOn the market NEOFOOT D403770033655NEOFOO2023NFJWOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Market distribution

Primary placement in France; available across 1 country total.

Placed on the market in France; per-country availability dates not published.

Device identification

Trade name: barre 21
UDI-DI code: 03770033655030
Basic UDI-DI: 3770033655NEOFOO2023NFJW
Reference / catalog number: NEO2023NFB21
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Barre longueur 21 NEOFOOT
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y0699EXTERNAL PROSTHESES AND ORTHOSES - OTHER

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

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