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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 1076 to 1100
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Cancellation or suspensionRegulatory action due to Failure to comply with a request for information within the specified period, effective 07/10/2020
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Cancellation or suspensionRegulatory action due to Failure to comply with a request for information within the specified period, effective 07/10/2020
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Cancellation or suspensionRegulatory action due to The sponsor failed to provide information requested by the Secretary therefore the sponsor failed to comply with an automatic condition of inclusion under paragraph 41FN(3)(c) of the Act., effective 07/10/2020
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Cancellation or suspensionRegulatory action due to The device is incorrectly classified therefore the certification made by the sponsor under paragraph 41FD(c) of the Act in the application for inclusion is incorrect., effective 07/10/2020
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Cancellation or suspensionRegulatory action due to The sponsor failed to provide information requested by the Secretary therefore the sponsor failed to comply with an automatic condition of inclusion under paragraph 41FN(3)(c) of the Act., effective 07/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 01/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 01/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 01/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 01/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 01/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 01/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 01/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 01/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 01/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 01/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 01/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 30/09/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 30/09/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 30/09/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 30/09/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 30/09/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 30/09/2020
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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 in the application for inclusion is incorrect., effective 28/09/2020
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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 in the application for inclusion is incorrect., effective 23/09/2020
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Cancellation or suspensionRegulatory action due to It appeared to the Secretary that the quality, safety or efficacy of the goods was unacceptable., effective 18/09/2020