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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

Mobile Dream tablettes de… — Class I MDR by LAZELEC

MD Atlas
LAZELEC

EUDAMED last updated this device on Apr 29, 2024

Mobile Dream tablettes de transfert abdominale gachette droite vert

376040090MOBILE-DREAM6R

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: LAZELEC
UDI-DI code: 03760400900795
Reference / catalog number: Mobile Dream tablettes de transfert abdominale gachette droite vert

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Manufacturer information

Organization name: LAZELEC
SRN: FR-MF-000007150
Manufacturer status: Active

Critical warnings

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

CW010
Lire la notice d'utilsation avant usage

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: Mobile Dream tablettes de transfert abdominale gachette droite vert
UDI-DI code: 03760400900795
Basic UDI-DI: 376040090MOBILE-DREAM6R
Reference / catalog number: Mobile Dream tablettes de transfert abdominale gachette droite vert
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: Fauteuil roulant pour personnes à mobilité réduite permettant d'accéder à des terrains accidentés
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y122199WHEELCHAIRS - 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

Related devices

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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.