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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 1051 to 1075
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Cancellation or suspensionRegulatory action due to Non response to s41JA, effective 19/10/2020
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Cancellation or suspensionRegulatory action due to The sponsor failed to provide information to comply with Essential principles of s41FN(3)(a), failed to provide evidence that device complies with conformity assessment procedures of s41FN(3)(b) and certifications made by the sponsor under section s41FC(2) of the Therapeutic Goods Act 1989 in relation to the inclusion of the kind of device in the ARTG are incorrect in a material particular., effective 16/10/2020
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Cancellation or suspensionRegulatory action due to The medical 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 14/10/2020
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Cancellation or suspensionRegulatory action due to Sponsor requested in writing the cancellation of the kind of device from the Register, effective 12/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 12/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 12/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 12/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 12/10/2020
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Cancellation or suspensionRegulatory action due to The safety and performance of the kind of device is unacceptable, effective 12/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 12/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 09/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 09/10/2020
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Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 09/10/2020
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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 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 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 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 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 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 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