Saltair is compliant Medical Device Class I with Food and Drugs Act (FDA) and Health Canada Medical Device Regulations.
Saltair device is manufactured and controlled by ISO 9001 Certified Management System and conform to all aspects of the agreed specification. This device complies with the essential requirements and provisions of European Council Directive MDD 93/42/EEC for Medical Device Class I and conform to standards: IEC60601-1: 2005/EN 60601-1: 2006, IEC/EN 60601-1-2: 2007, CE Marking.
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Saltair Product Demonstration
SaltAir – A Natural Home Relief in Asthma