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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

EASY-UP — Class I MDR by France Reval

MD Atlas
France Reval

EUDAMED last updated this device on Apr 15, 2026

EASY-UP

3666401TF002QW

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: France Reval
UDI-DI code: 36664010011378
Reference / catalog number: 5496.00

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Manufacturer information

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

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Critical warnings

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

CW999
Comprendre le manuel d'utilisation avant la première utilisation. Toujours planifier les opérations de levage avant de commencer. Toujours utiliser les sangles livrées avec l'appareil ou se renseigner de la compatibilité. Toujours vérifier que la sangle est adaptée au patient. Ne jamais utiliser une sangle abimée. Toujours actionner les freins avant de soulever un patient.

Market distribution

Primary placement in France; available across 2 countries total.

Country	On market since	Until
FrancePrimary placement		Still on market
Italy	Apr 30, 2015	Still on market

Device identification

Trade name: EASY-UP
UDI-DI code: 36664010011378
Basic UDI-DI: 3666401TF002QW
Reference / catalog number: 5496.00
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 verticalisateur permet de façon simple et ergonomique de relever un patient et d'alléger la pesanteur de son corps.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V0805030102ELECTRIC MOBILE LIFTS

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

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.