Unregistered Medical Device
The Food and Drug Agency (FDA) warns all healthcare professionals and the general public against the purchase and use of the unregistered medical device:1:->INNOSPIRE MINI WITH SIDESTREAM PLUS
The FDA verified through post-marketing surveillance that the abovementioned medical device is not registered and the Certificate of Product Registration (CPR) has not yet been issued. Pursuant to the Republic Act No. 9711, otherwise known as the “Food and Drug Agency Act of 2009”, the manufacture, importation, exportation, sale, offering for sale, distribution, transfer, non-consumer use, promotion, advertising or sponsorship of health products without the proper authorization is prohibited.