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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 ESCAMOTABLE CANOLI pour lit… — Class I MDR

MD Atlas
ALTER ÉCO SANTÉ SAS

EUDAMED last updated this device on Aug 22, 2024

BARRE ESCAMOTABLE CANOLI pour lit médicalisé

376031137CANOLI39

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ALTER ÉCO SANTÉ SAS
UDI-DI code: 03760311370373
Reference / catalog number: DECLIBAR90

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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 ESCAMOTABLE CANOLI pour lit médicalisé
UDI-DI code: 03760311370373
Basic UDI-DI: 376031137CANOLI39
Reference / catalog number: DECLIBAR90
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 ESCAMOTABLE CANOLI pour lit médicalisé
Additional information URL: https://www.alterecosante.net/fr/product/barre-escamotable-canoli/
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

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.

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