Air Liquide Medicinal, S.A.
Portugal PT-MF-000004888 Last updated 17 Sep 2026
- Devices
- 2
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
EUDAMED certificates
Notified body 1639 1 certificate
- ES25/00001061 Issued
Quality management system EU MDR
- Issued
- 13 Oct 2025
- Expires
- 13 Oct 2030
Related companies
Notified bodies
- Notified body 1639
What Air Liquide Medicinal, S.A. makes
Air Liquide Medicinal, S.A. manufactures medical gas distribution systems designed for hospital and clinical environments, ensuring controlled delivery of therapeutic gases like oxygen, nitrogen, and medical air.
These systems are classified as Class IIa medical devices and are registered in the EU’s eudamed database. The company is based in Portugal.
Frequently asked questions
What types of medical devices does Air Liquide Medicinal, S.A. manufacture?
Air Liquide Medicinal, S.A. specialises in medical gas distribution systems tailored for hospitals and clinical settings. These systems are engineered to deliver therapeutic gases—such as oxygen, nitrogen, and medical air—in a controlled and precise manner, ensuring safe administration to patients.
Where is Air Liquide Medicinal, S.A. based?
The company is headquartered in Portugal, where it operates as a manufacturer of medical devices. Its focus on local production aligns with regulatory compliance and logistical efficiency for European markets.
Which regulatory registries list Air Liquide Medicinal, S.A.’s devices?
Air Liquide Medicinal, S.A.’s medical gas distribution systems are listed in the eudamed database, the official EU registry for medical devices. This registration reflects compliance with EU Medical Device Regulations (MDR) or previous directives, ensuring transparency and traceability for healthcare providers.
How are Air Liquide Medicinal, S.A.’s devices classified under EU regulations?
The company’s medical gas distribution systems fall under Class IIa classification. This classification is determined by factors such as the device’s intended use, potential risks, and the level of intervention required for patient therapy. Class IIa devices undergo stricter design controls and clinical evaluations compared to Class I but are not as high-risk as Class IIb or III devices.
Information
- Country
- Portugal
- Address
- R. Dr. António Loureiro Borges, nº4 - 3º - Arquiparque - Miraflores 1495-131 Algés - Portugal, Algés, Portugal
- Website
- airliquide.com
- [email protected]
- EUDAMED SRN
- PT-MF-000004888