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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

BARRE LATERALE DE REDRESSEMENTCANO… — Class I MDR

MD Atlas
ALTER ÉCO SANTÉ SAS

EUDAMED last updated this device on Aug 22, 2024

BARRE LATERALE DE REDRESSEMENTCANOLI RAL5002 pour lit traditionnel largeur max. 140 cm

376031137CANOLI39

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ALTER ÉCO SANTÉ SAS
UDI-DI code: 03760311370502
Reference / catalog number: DEBARCOUL140.02

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Manufacturer information

Organization name: ALTER ÉCO SANTÉ SAS
SRN: FR-MF-000003051
Manufacturer status: Active

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW010
ATTENTION AU KIT DE FIXATION
CW018
ATTENTION AU KIT DE FIXATION

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: BARRE LATERALE DE REDRESSEMENTCANOLI RAL5002 pour lit traditionnel largeur max. 140 cm
UDI-DI code: 03760311370502
Basic UDI-DI: 376031137CANOLI39
Reference / catalog number: DEBARCOUL140.02
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: BARRE LATERALE DE REDRESSEMENTCANOLI pour lit traditionnel largeur max. 140 cm COULEUR BLEU OUTREMER
Additional information URL: https://www.alterecosante.net/fr/product/barre-laterale-de-redressement-canoli-fuschia-bleue/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12019010PATIENT TRANSFER SYSTEMS

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.