Linde France
France FR-MF-000000961 Last updated 21 Oct 2026
- Devices
- 5
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Argon médical chirurgical Ref 12040128
Visiostar 3 Ref R613938
Protoxyde d'azote cryogénique médical Ref 3680102
Visiostar 2 Ref R613931
EUDAMED certificates
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
Related companies
Notified bodies
About
Online store for healthcare professionals. Medical gas control 24/7. Historical 1 year documents.
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.
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.
Information
- Country
- France
- Address
- Les Jardins du Lou Bâtiment 5, Lyon Cedex 07, France
- Website
- www.linde-healthcare.fr
- [email protected]
- Phone
- +33 810 421 000
- PRRC contact
- Sara RENAUX
- EUDAMED SRN
- FR-MF-000000961