Philips Electronics Australia Ltd

Regulatory action due to The sponsor has provided information or documents in response to a notice under section 41JA to the effect that medical devices of that kind are not being supplied in Australia, imported into Australia or exported from Australia., effective 19/07/2017

Regulatory action due to The sponsor has provided information or documents in response to a notice under section 41JA to the effect that medical devices of that kind are not being supplied in Australia, imported into Australia or exported from Australia., effective 19/07/2017

Regulatory action due to 6 monthly suspension of the device under paragraph 41GA(1)(a)(i) of the Act due to the potential risk of death, serious illness or serious injury if the kind of device continues to be included in the ARTG., effective 16/05/2017