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Action
- Medical device cancellation (827)
- Medicine suspension (472)
- Complementary medicine cancellation (203)
- Medical device suspension (86)
- Medicine cancellation (59)
- Revocation of a TGA issued Conformity Assessment Certificate (51)
- Medical device cancellation - certain devices within an entry (22)
- Registered medicine cancellation (12)
- Voluntary revocation at the request of the manufacturer (9)
- Medical device cancellation - requested by the sponsor - certain devices within an entry (8)
- Medical device cancellation (7)
- Listed medicine cancellation (3)
- Listed medicine cancellation (3)
- Revocation of a TGA issued Conformity Assessment Certificate. (3)
- Revocation of medical device suspension (2)
- Revoked medicine suspension (2)
- Medical device cancellation (1)
- Medical device cancellation – certain devices within an entry (1)
- Suspension from the ARTG under subsection s41GA(1)(b) (1)
- Voluntary revocation at the request of the manufacturer. (1)
Find out more about Cancellations and Suspensions.
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1780 result(s) found, displaying 1001 to 1025
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Cancellation or suspensionRegulatory action due to The sponsor failed to respond to a request for information and therefore failed to comply with an automatic condition of inclusion., effective 23/11/2020
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Cancellation or suspensionRegulatory action due to Failure to comply with a condition of inclusion, effective 20/11/2020
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Cancellation or suspensionRegulatory action due to The sponsor has failed to comply with an automatic condition of inclusion applied to this ARTG entry under subsection 41FN(5A) of Therapeutic Goods Act 1989 and regulation 5.11 of Therapeutic Goods (Medical Devices) Regulations 2002, to provide information about the safety and performance of the Devices by 1 October each year for three consecutive years after the inclusion., effective 20/11/2020
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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, that the Product in question is a medical device, is incorrect., effective 16/11/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 12/11/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 12/11/2020
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Cancellation or suspensionRegulatory action due to Under subsection 41GA(1)(b); it is likely that there are grounds for cancelling this kind of device from the ARTG under subsection 41GN(1)(b) & (1)(e)., effective 11/11/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 07/11/2020
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Cancellation or suspensionRegulatory action due to The product is not a therapeutic good/medical device therefore the certification made by the sponsor under paragraph 41FD(a) of the Act in the application for inclusion is incorrect., effective 06/11/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 06/11/2020
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Cancellation or suspensionRegulatory action due to Medical devices of that kind are not being supplied in Australia, imported into Australia or exported from Australia, effective 06/11/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 06/11/2020
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Cancellation or suspensionRegulatory action due to Medical devices of that kind are not being supplied in Australia, imported into Australia or exported from Australia, effective 06/11/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 06/11/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 06/11/2020
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Cancellation or suspensionRegulatory action due to The product is not a therapeutic good/medical device therefore the certification made by the sponsor under paragraph 41FD(a) of the Act in the application for inclusion is incorrect., effective 06/11/2020
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Cancellation or suspensionRegulatory action due to The sponsor failed to comply with a notice under section 41JA of the Act and therefore failed to comply with an automatic condition of inclusion under s41FN(3)(c)of the Act., effective 04/11/2020
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Cancellation or suspensionRegulatory action due to The sponsor failed to comply with the conditions of inclusion stipulated under paragraph 41FN of the Therapeutic Goods Act 1989., effective 03/11/2020
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Cancellation or suspensionRegulatory action due to The sponsor failed to provide information requested by the TGA under section 41JA of the Act. The sponsor therefore failed to comply with an automatic condition of inclusion (s41FN(3)(c) of the Act)., effective 03/11/2020
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Cancellation or suspensionRegulatory action due to The sponsor failed to provide information requested by the TGA under section 41JA of the Act. The sponsor therefore failed to comply with an automatic condition of inclusion (s41FN(3)(c) of the Act)., effective 03/11/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 02/11/2020
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Cancellation or suspensionRegulatory action due to The product is an excluded good for the purposes of the Act, that is, the product is determined not to be a therapeutic good. Therefore the certification made by the sponsor under paragraph 41FD(a) of the Act in the application for inclusion, that the product is a medical device, is incorrect., effective 28/10/2020
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Cancellation or suspensionRegulatory action due to The suspension of the Device from the ARTG was not revoked before the expiry date of the suspension., effective 27/10/2020
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Cancellation or suspensionRegulatory action due to The suspension of the Device from the ARTG was not revoked before the expiry date of the suspension., effective 27/10/2020
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Cancellation or suspensionRegulatory action due to The suspension of the Device from the ARTG was not revoked before the expiry date of the suspension., effective 27/10/2020