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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

TRANSALT SOUPLE — Class I MDR by ALTER ÉCO SANTÉ SAS

MD Atlas
ALTER ÉCO SANTÉ SAS

EUDAMED last updated this device on Aug 21, 2024

TRANSALT SOUPLE

376031137TRANSALT2Q

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ALTER ÉCO SANTÉ SAS
UDI-DI code: 03760311370908
Reference / catalog number: SI21700

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Manufacturer information

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

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.

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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: TRANSALT SOUPLE
UDI-DI code: 03760311370908
Basic UDI-DI: 376031137TRANSALT2Q
Reference / catalog number: SI21700
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: Matelas de transfert en position couchée souple et enroulable compatible avec tous les relève-buste et avec le stockage en ambulance
Additional information URL: https://www.alterecosante.net/fr/product/matelas-de-transfert-transalt/
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

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

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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.