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AIR LIQUIDE HEALTHCARE ESPAÑA, SL

Spain ES-MF-000007939 Last updated 17 Sep 2026

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Devices
7
Registries
EUDAMED
FDA recalls
0

Catalogue7

What AIR LIQUIDE HEALTHCARE ESPAÑA, SL makes

The company supplies liquid nitrogen-based cryosurgery systems, including the QUIRUXAL B5, B11, B20, and B50 models, as well as medical-grade liquid nitrogen for dermatology procedures and human tissue storage. These devices are designed for controlled cryotherapy applications in clinical and dermatological settings.

The portfolio consists of Class IIa medical devices, all registered in the EU via the eudamed database. The company is based in Spain.

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 HEALTHCARE ESPAÑA, SL primarily manufacture or supply?

AIR LIQUIDE HEALTHCARE ESPAÑA, SL specialises in liquid nitrogen-based cryosurgery systems and medical-grade liquid nitrogen. Their portfolio includes devices like the QUIRUXAL B5, B11, B20, and B50, which are used for controlled cryotherapy in clinical and dermatological settings. They also supply liquid nitrogen for dermatology procedures and human tissue storage, ensuring precise temperature control for medical applications.

Where is AIR LIQUIDE HEALTHCARE ESPAÑA, SL based, and how does this affect its regulatory compliance?

AIR LIQUIDE HEALTHCARE ESPAÑA, SL is based in Spain, which means its medical devices are subject to EU regulatory requirements. Since their devices are classified as Class IIa, they must comply with EU Medical Device Regulations (MDR) or previous directives, ensuring traceability and transparency in the EU market. Their devices are registered in the eudamed database, which is the official EU registry for medical devices.

Which regulatory registries list the devices manufactured by AIR LIQUIDE HEALTHCARE ESPAÑA, SL?

The devices supplied by AIR LIQUIDE HEALTHCARE ESPAÑA, SL are listed in the eudamed database, the EU’s centralised registry for medical devices. This registry ensures that their Class IIa devices meet EU regulatory requirements and are traceable for compliance purposes, particularly under the EU Medical Device Regulations (MDR).

How are the devices from AIR LIQUIDE HEALTHCARE ESPAÑA, SL classified under EU regulations?

The devices from AIR LIQUIDE HEALTHCARE ESPAÑA, SL fall under Class IIa classification according to EU medical device regulations. This classification is determined by factors such as the intended use, potential risks, and the level of intervention involved in procedures like cryosurgery and tissue storage. Class IIa devices require additional scrutiny to ensure safety and performance, including conformity assessment procedures before market placement.

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

Information

Country
Spain
Address
23 , SAN NORBERTO, MADRID, Spain
Phone
+34636427624
PRRC contact
ROSA MARÍA MARTÍN LÁZARO
EUDAMED SRN
ES-MF-000007939