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Date
Sponsor content
2 result(s) found, displaying 1 to 2
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Cancellation or suspensionRegulatory action due to The product is not a medical device. Therefore, the certification made by the sponsor under paragraph 41FD(a) of the Act in the application for inclusion is incorrect., effective 14/08/2020
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Cancellation or suspensionRegulatory action due to The good had become an exempt good under Schedule 5, Item 8(f) of the Regulations. Exempt goods are not required to be included on the ARTG (paragraph 18(1) of the Act)., effective 18/06/2020