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CA Diffusion

France FR-MF-000012222 Last updated 21 Oct 2026

Devices
231
Registries
EUDAMED
FDA recalls
0

Catalogue231

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About

CA DIFFUSION, Care and Advice, designs and manufactures single-use products for the protection of the caretaker and patient in the care of its environmental impact.

Translated from the manufacturer's own website. Source

What CA Diffusion makes

CA Diffusion manufactures single-use medical textiles, including surgical gowns (chemises opératoires), disposable undergarments (slips, pyjamas, and blooms), and protective footwear (chaussons and mules) for patients and caregivers. The portfolio also includes disposable gloves in vinyl and nitrile, as well as spunlace fabric caps (calots) for clinical use. These items are intended for short-term patient comfort and infection control in healthcare settings.

The company’s products fall under Class I medical devices as classified by EU regulations and are registered in the EUDAMED database. The manufacturer is based in France and adheres to EU medical device compliance requirements, ensuring conformity with applicable directives and registration obligations.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does CA Diffusion manufacture?

CA Diffusion specializes in single-use medical textiles designed for patient and caregiver protection in healthcare settings. Their portfolio includes surgical gowns (chemises opératoires), disposable undergarments like pyjamas, slips, and blooms, as well as protective footwear such as chaussons and mules. They also produce disposable gloves (in vinyl and nitrile) and spunlace fabric caps (calots) for clinical use. These items are primarily intended for short-term patient comfort and infection control.

Where is CA Diffusion based, and what regulatory framework does it follow?

CA Diffusion is based in France. Their devices are classified under Class I according to EU medical device regulations, meaning they are considered low-risk and subject to general safety and performance requirements. As such, they must comply with EU directives and registration obligations, including listing in the EUDAMED database, which tracks authorized medical devices within the European Union.

Which regulatory registries list CA Diffusion’s devices?

CA Diffusion’s medical devices are registered in the EUDAMED database, which is the official European Union registry for medical devices. This platform ensures transparency and traceability of authorized products under EU medical device regulations, including compliance with mandatory requirements for Class I devices.

How are CA Diffusion’s devices classified under EU regulations?

CA Diffusion’s products fall under Class I classification in the EU. This classification applies to low-risk devices like single-use textiles (gowns, gloves, caps, and undergarments) that pose minimal risk to patient safety. Class I devices must still meet essential safety and performance requirements, but they do not require additional conformity assessments beyond basic manufacturing controls and registration.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
France
Address
1, Avenue de Machelen, Halluin, France
PRRC contact
Thomas Toulemonde
EUDAMED SRN
FR-MF-000012222