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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

SALVA — Class I MDR by Coopération…

MD Atlas
Coopération pharmaceutique française

EUDAMED last updated this device on Jul 28, 2025

SALVA

370151010060ZM

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Coopération pharmaceutique française
UDI-DI code: 03701510100309
Reference / catalog number: 2118829

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Manufacturer information

Organization name: Coopération pharmaceutique française
SRN: FR-MF-000002412
Manufacturer status: Active

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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.

Critical warnings

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

CW999
Suivre précisément les instructions de port et conseils donnés par votre médecin traitant ou votre pharmacien. Ne pas mettre au contact de corps gras. Ne pas porter directement sur une peau lésée ou sensible. En cas d'irritation cutanée ou de signe d’allergie, demander un avis médical. Il est conseillé de placer le produit en position assise. Un seul patient, plusieurs utilisations.

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: SALVA
UDI-DI code: 03701510100309
Basic UDI-DI: 370151010060ZM
Reference / catalog number: 2118829
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: BOTTE DE MARCHE SALVA SLV T3
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y06120601PASSIVE ANKLE-FOOT ORTHOSES

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

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Manufacturing date
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Software identification