Airpro systems components are certified for compliance with the ISO 9001:2015 and for medical devices upgraded to ISO 13485:2003.

Our oxygen and nitrogen generators are manufactured according to PED (Pressure Equipment Directive) and MDD (Medical Device Directive) rules and regulations.

AirPro Oxygen Generators and have been designed and supplied in accordance with the following Medical Oxygen Standards: USP XXII, CE 93/42/EEC, CSA, HTM2022, and the Argentinian Medical Oxygen Standards.

AirPro Oxygen Generators are manufactured according to the quality standards and regulations of:

Ph.Eur. (The European Pharmacopoeia)

ASME (American Society of Mechanical Engineers)

PED (Pressure Equipment Directive)

MDD (Medical Device Directive)

ASME (American Society of Mechanical Engineers)

Airpro Medical Oxygen Systems meet ISO10083 and ISO7396 criteria for Oxygen Pressure and ISO8573(Class 1.4.1) for Air Quality.

When using Nitrogen for the packaging of pharmaceutical products, we understand you want assurance that the Nitrogen you’re using is reliable, traceable and compliant with regulations. Since gases used in packaging come into direct contact with Active Product Ingredients (APIs), it is important that the gas you use is compliant with the requirements of European directives relating to the use and quality of APIs.

AirPro Nitrogen Generators are manufactured according to the standards and regulations of:

Ph.Eur. (The European Pharmacopoeia)

NSAI (National Standards Authority of Ireland)

ASME (American Society of Mechanical Engineers)

PED (Pressure Equipment Directive)

MDD (Medical Device Directive)