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Air Liquide developed its strategy for medical gases, which are classified as medicine in a growing number of counties, while researching new technological applications for gases and new products. Air Liquide also offers a number of services to ensure continuous gas supplies, quality and optimum conditions of safety. The most common gases in healthcare are: oxygen, nitrogen, nitrous oxide, carbon dioxide, compressed air and others. All of these gases are offered by Air Liquide.

Oxygen, as a basic component of air and necessary to sustain life and produce energy is essential in many healthcare applications. In hospitals medical oxygen plays a vital role in nearly all medical procedures:

• anesthesiology,
• surgery,
• resuscitation,
• intensive care,
• tissue reconstruction,
• pain management.

In patient's homes, it is indispensable in treating respiratory insufficiency (oxygen therapy).

In May 2000, Air Liquide was the first company in Poland to gain the concession for medical oxygen manufacturing as well as the Registration Certificate for medical oxygen, which was inscribed to the register of pharmaceutical and medical remedies.
We offer deliveries of medical oxygen in compressed or liquid form. Cylinders can be supplied individually or linked together in bundles of cylinders, which then empty as if they were a single container. Air Liquide has for many years introduced innovative solutions for gas cylinders to improve their safety, economy and ease of use.

For cryotherapy and cryosurgery, Air Liquide in Poland offers liquid nitrogen with the equipment for its storing, transport and application.

Air Liquide Group also works to make medical gases easier to use. We design and manufacture anaesthesia and resuscitation equipment, aerosol therapy and sleep apnea devices.

The manufacturing site of Air Liquide in Poland has been granted a certificate of Good Manufacturing Practice (GMP) compliance. It results that we comply with the GMP requirements laid down in Directive 2003/94/EC and fulfil the recommendations of World Health Organization (WHO).

Good Manufacturing Practice is the quality system regulation including requirements related to the methods used in, and the facilities and controls used for, designing, manufacturing, packaging, labelling, storing, installing, and servicing of medical devices intended for human use.

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