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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

Coiffe à nouer Spunlace Bleu — Class I MDR by CA Diffusion

MD Atlas
CA Diffusion

EUDAMED last updated this device on Nov 5, 2025

Coiffe à nouer Spunlace Bleu

376006117COIFFSPUN7X

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: CA Diffusion
UDI-DI code: 03760061178397
Reference / catalog number: CA1710SL

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Manufacturer information

Organization name: CA Diffusion
SRN: FR-MF-000012222
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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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: Coiffe à nouer Spunlace Bleu
UDI-DI code: 03760061178397
Basic UDI-DI: 376006117COIFFSPUN7X
Reference / catalog number: CA1710SL
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: 100
Additional product description: Cette coiffe à nouer en Spunlace offre une protection optimale tout en assurant confort et respirabilité. Grâce à sa matière douce et légère, elle limite la transpiration et favorise une aération continue, même lors d'un port prolongé. Sa conception ergonomique permet de couvrir efficacement le front et les côtés de la tête, tout en s'ajustant parfaitement grâce aux liens de serrage. Idéale pour les professionnels de santé, elle garantit un maintien sécurisé et un confort durable lors des interventions en milieu médical.
Additional information URL: No additional information URL provided by the manufacturer.
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.

T0207CAPS AND HEADWEAR (EXCLUDING PERSONAL PROTECTIVE EQUIPMENT - PPE)

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.