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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

CAPRICE — Class I MDR by France Reval

MD Atlas
France Reval

EUDAMED last updated this device on Feb 5, 2026

CAPRICE

3666401BAWR003MC

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: France Reval
UDI-DI code: 36664010023944
Reference / catalog number: 7100.1GS71R

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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 la manuel d'utilisation avant la première utilisation. Modification de la baignoire interdite. Ne jamais laisser un patient sans surveillance. Ne jamais dépasser la charge maximale. NE pas utiliser d'objet électrique dans la zone de bain. Toujours vérifier la température de l'eau avant le bain. Ne pas rester sous la baignoire lors de la descente. Vérifier le bon accrochage du siège avant d'activer le lève personne. Ne pas dépasser le niveau du trop plein.

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: CAPRICE
UDI-DI code: 36664010023944
Basic UDI-DI: 3666401BAWR003MC
Reference / catalog number: 7100.1GS71R
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: La baignoire à hauteur variable CAPRICE est conçue pour les patients à mobilité réduire afin de leur permettre de bénéficier d'un bain sécurisé.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y093399WASHING, BATHING AND SHOWERING DEVICES - 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

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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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.