well I think you might want to take another look... you might be having trouble seeing things, your telling me you don't see the word "medical device" anywhere in this certificate? its even in the document name.. LOL its called "CertificateofMedicalDevice.pdf"
(1) PURPOSE OF THE LAW AND SYSTEM
The objective of this law is to regulate matters necessary for securing the quality, efficacy and safety of pharmaceuticals, quasi-drugs (Iyaku-bugaihin), cosmetics and medical devices, while taking necessary steps to promote research and development of pharmaceuticals and medical devices in high necessity, and thereby improve public better health and hygiene.
(2) OUTLINE OF THE LAW AND SYSTEM
The Pharmaceutical Affairs Law subjects pharmaceuticals, quasi-drugs, and medical devices to various approval and permit systems, such as licence for marketing authorization holder and manufacture, marketing approval, pharmacy establishment permits, and pharmaceuticals and medical devices selling business permits, to ensure efficacy and safety of the products (Articles 4, 12, 13, 14, 24 and 39). In addition, prohibition of extravagant advertisement (Article 66), on-the-spot inspections by a supervisory agency (Article 69), a duty to reports on adverse reaction and etc. (Article 77-4-2) apply to pharmaceuticals, quasi-drugs, and medical devices.