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Organization name
UDI-DI code
Reference / catalog number

BRANCARD DE DOUCHE MURAL A… — Class I MDR by France Reval

MD Atlas
France Reval

EUDAMED last updated this device on Mar 9, 2026

BRANCARD DE DOUCHE MURAL A HAUTEUR VARIABLE ELECTRIQUE

3666401DC005JX

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: France Reval
UDI-DI code: 36664010001478
Reference / catalog number: 7755.00

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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
Lire la notice d'utilisation. Ne jamais laisser le patient sans surveillance. Ne jamais dépasser la charge maximale d'utilisation. Vérifier que les barrières de sécurité soient verrouillées. Ne jamais utiliser de matelas abimé. Ne jamais positionner le patient en extrémité de plateau. Deux soignants doivent être présent lors du transfert du 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: BRANCARD DE DOUCHE MURAL A HAUTEUR VARIABLE ELECTRIQUE
UDI-DI code: 36664010001478
Basic UDI-DI: 3666401DC005JX
Reference / catalog number: 7755.00
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: Ce brancard est destiné à la douche des patients. Brancard à hauteur variable fixé au mur. Avec relève buste et inclinaison plateau.
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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Manufacturing date
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