CA-MI srl

CA-MI is a family-run company founded in 1984 and specialized in the production of SURGICAL Aspirators, Aerosol Therapy Equipment and Thermal Inhalers. Over the years we have expanded our range of products becoming a reference brand both in the professional hospital sector and in the home-care sector in pharmacies and healthcare. Marketing and distribution in the Italian and international markets can count on a vast network of distributors, resellers and representative agents. Recent and important investments have allowed us to offer new products, innovative designs, cutting-edge technologies and a service with continuously improving response times to the various market segments. At the same time, we keep our research and development departments constantly active for a continuous improvement of existing devices and for the implementation and completion of existing ranges.

About Us

All devices are manufactured under  UNI EN ISO 9001: 2015 and EN ISO 13485: 2016 quality systems and are certified with the notified body T Ü V SÜD Product Service GmbH (CE 0123).

We invite you to visit us at the major national and international trade fairs such as Medica in Düsseldorf or Arab Health in Dubai, where we are constantly present with our stand and our entire production.

Class IIa devices compliant with Directive 93/42 / EEC (and subsequent amendments): Devices for Aerosol Therapy, Accessory Kits for Aerosol Therapy, Surgical Suction Units, Electric Breast Pump, Thermal Inhaler, Pressure Monitors, Pulse Oximeter, Electric Thermometers, Infrared Thermometers and Tens.  

Non-sterile Class I devices compliant with Directive 93/42 / EEC (and subsequent amendments):  Breathing Incentives, Anti-decubitus Mattress, Compression Stockings.

Class Im devices (measurement function) compliant with Directive 93/42 / EEC (and subsequent amendments):  Containers for Aspirated Liquids, Disposable Bags, Aneroid and Handheld Sphygmomanometers, Mercury-free Clinical Thermometers.

Certificates

CA-MI constantly keeps its research and development departments active for a continuous improvement of existing devices and for the implementation and completion of existing ranges. 
All devices are manufactured under  UNI EN ISO 9001: 2015 and EN ISO 13485: 2016 quality systems and are certified with the notified body T Ü V SÜD Product Service GmbH (CE 0123) and the Declarations of Conformity are available on request at the regulatory department.