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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

BAIN MEMBRES SUPERIEURS — Class I MDR by France Reval

MD Atlas
France Reval

EUDAMED last updated this device on Mar 12, 2026

BAIN MEMBRES SUPERIEURS

3666401DC011JS

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: France Reval
UDI-DI code: 36664010002840
Reference / catalog number: 1324.00

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Manufacturer information

Organization name: France Reval
SRN: FR-MF-000011523
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW999
Comprendre le manuel d'utilisation avant utilisation. Ne jamais laisser le patient sans surveillance. Toujours vérifier la température de l'eau avant le contact du patient avec l'eau.

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: BAIN MEMBRES SUPERIEURS
UDI-DI code: 36664010002840
Basic UDI-DI: 3666401DC011JS
Reference / catalog number: 1324.00
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: Le bain de membres supérieurs permet la rééducation des poignets ou des coudes ou la vasodilatation ou la vasoconstriction des membres supérieurs.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12069080VARIOUS PHYSIOTHERAPY AND REHABILITATION INSTRUMENTS - HARDWARE ACCESSORIES

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

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

BAGHEERA3666401BA002HMOn the market BAGHEERA3666401BA002HMOn the market BAIGNOIRE GRANDS BRULÉS3666401GB001KHOn the market BAIN DE MEMBRES INFERIEURS3666401DC009K7On the market BAIN DE MEMBRES INFERIEURS3666401DC009K7On 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.