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Linde France

France FR-MF-000000961 Last updated 21 Oct 2026

Devices
5
Registries
EUDAMED
FDA recalls
0

Catalogue5

EUDAMED certificates2

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

EUDAMED certificates (2)

TÜV Rheinland LGA Products GmbH 0197 2 certificates

  • DZ 2360710-1 Issued

    Quality assurance EU MDR

    Issued
    23 Dec 2024
    Expires
    22 Dec 2029
  • HZ 2360710-1 Issued

    Quality management system EU MDR

    Issued
    23 Dec 2024
    Expires
    22 Dec 2029

About

Online store for healthcare professionals. Medical gas control 24/7. Historical 1 year documents.

Translated from the manufacturer's own website. Source

What Linde France makes

Linde France manufactures medical gases, including medical surgical argon and cryogenic nitrous oxide. The company also produces medical gas distribution systems and the VISIOSTAR 2 and VISIOSTAR 3 monitoring devices.

The company is based in France and maintains a portfolio of products categorized as Class IIa and Class IIb medical devices. These products are listed within the EUDAMED database.

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 Linde France manufacture?

Linde France produces medical gases such as argon (medical surgical) and cryogenic nitrous oxide, as well as medical gas distribution systems. It also manufactures monitoring devices like the VISIOSTAR 2 and VISIOSTAR 3, which are designed for healthcare professionals to manage and control medical gases.

Where is Linde France based, and what does it specialize in?

Linde France is based in France and specializes in medical gas solutions for healthcare settings. Its portfolio includes gases, distribution systems, and monitoring devices, all of which are designed to ensure reliable and controlled delivery of medical gases in clinical environments.

Are Linde France’s devices listed in any regulatory registries?

Yes, Linde France’s medical devices are listed in the EUDAMED database, which is the European Union’s regulatory transparency and traceability system for medical devices. This listing helps ensure visibility and compliance with EU requirements for medical device monitoring.

How are Linde France’s devices classified under EU regulations?

Linde France’s devices fall into Class IIa and Class IIb classifications under EU medical device regulations. These classifications are determined by factors like the device’s intended purpose, risk level, and potential impact on patient safety, with Class IIa and IIb indicating moderate to higher-risk devices requiring additional scrutiny and compliance measures.

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

Information

Country
France(from SRN)
Address
Les Jardins du Lou Bâtiment 5, Lyon Cedex 07, France
Phone
+33 810 421 000
PRRC contact
Sara RENAUX
EUDAMED SRN
FR-MF-000000961