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Air Liquide Medicinal, S.A.

Portugal PT-MF-000004888 Last updated 17 Sep 2026

Devices
2
Registries
EUDAMED
FDA recalls
0

Catalogue2

EUDAMED certificates1

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

EUDAMED certificates (1)

Notified body 1639 1 certificate

  • ES25/00001061 Issued

    Quality management system EU MDR

    Issued
    13 Oct 2025
    Expires
    13 Oct 2030

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.

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 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.

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

Information

Country
Portugal(from SRN)
Address
R. Dr. António Loureiro Borges, nº4 - 3º - Arquiparque - Miraflores 1495-131 Algés - Portugal, Algés, Portugal
EUDAMED SRN
PT-MF-000004888