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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

BAIGNOIRE GRANDS BRULÉS — Class I MDR by France Reval

MD Atlas
France Reval

EUDAMED last updated this device on Mar 12, 2026

BAIGNOIRE GRANDS BRULÉS

3666401GB001KH

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: France Reval
UDI-DI code: 36664010002772
Reference / catalog number: 4854.00

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Manufacturer information

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

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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.

Critical warnings

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

CW999
Comprendre le manuel d'utilisation avant la première utilisation. Ne pas rester sous la baignoire lors de la descente. Ne pas utiliser d'objet électrique à proximité du bain. Toujours être préparé avant le transfert du patient. Vérifier la température de l'eau avant de mettre le patient.

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: BAIGNOIRE GRANDS BRULÉS
UDI-DI code: 36664010002772
Basic UDI-DI: 3666401GB001KH
Reference / catalog number: 4854.00
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: La baignoire pour grands brulés à hauteur variable électrique est destinée au bain et au soin des patients "grands brulés".
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

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