Results for
"[search-keyword]"
Sponsor content
2 result(s) found, displaying 1 to 2
-
Cancellation or suspensionRegulatory action due to The device was incorrectly classified as a class I medical device. From the information available the device should be included on the ARTG at a higher classification. Therefore, the certification made by the sponsor under paragraph 41FD(c) of the Act in the application for inclusion is incorrect., effective 30/01/2020
-
ARTGAustralian Register of Therapeutic Goods (ARTG) information for Dermal Solutions Australia atf Bodilite Systems Trust - Skin surface treatment system.