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Air Liquide Santé France

France FR-MF-000001204 Last updated 17 Sep 2026

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Devices
43
Registries
EUDAMED
FDA recalls
0

Catalogue43

EUDAMED certificates1

Held under this manufacturer's EUDAMED registration, grouped by notified body; in force first, then by expiry.

EUDAMED certificates (1)

GMED SAS 0459 1 certificate

  • 40258 Amended

    Quality management system EU MDR

    Issued
    30 Sep 2026
    Expires
    15 Nov 2027
    Reason
    Mnf data change

Notified bodies

About

Air Liquide Santé France is a company specialized in medical gases, equipment and value-added services throughout the santé care chain.

Translated from the manufacturer's own website. Source

What Air Liquide Santé France makes

The company manufactures medical-grade carbon dioxide (CO₂) gas cylinders and supplies designed for laparoscopy and colonoscopy procedures, including various pressure and volume configurations (e.g., B5, B20, V12) for use in Belgium, Luxembourg, the Netherlands, Denmark, Norway, and Sweden.

These devices fall under EU Class IIa classification and are registered in the eudamed database. The company is based in France.

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 Air Liquide Santé France manufacture?

Air Liquide Santé France specializes in medical-grade carbon dioxide (CO₂) gas cylinders and related equipment. These devices are specifically designed for use in laparoscopic and colonoscopic procedures, offering various pressure and volume configurations (e.g., B5, B20, V12) to meet regional requirements in countries like Belgium, Luxembourg, the Netherlands, Denmark, Norway, and Sweden.

Where is Air Liquide Santé France based?

The company is headquartered in France, where it develops and supplies medical gases and associated equipment for healthcare applications.

Which regulatory registries list Air Liquide Santé France’s devices?

The company’s medical CO₂ devices are registered in the eudamed database, which is the official EU registry for medical devices. This ensures transparency and compliance with EU regulatory requirements.

How are Air Liquide Santé France’s devices classified under EU regulations?

All listed medical CO₂ devices fall under EU Class IIa classification. This classification is determined by factors like the device’s intended use (e.g., minimally invasive procedures) and associated risks, requiring compliance with specific EU regulatory standards.

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

Information

Country
France
Address
6, Cognacq-Jay, Paris, France
Phone
0 969 328 133(from company website)
PRRC contact
Johan Huynh
EUDAMED SRN
FR-MF-000001204