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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 1 to 25
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Cancellation or suspensionRegulatory action due to voluntary revocation at the request of the manufacturer, effective 19/11/2024
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Cancellation or suspensionRegulatory action due to voluntary revocation at the request of the manufacturer, effective 2/09/2024
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Cancellation or suspensionRegulatory action due to voluntary revocation at the request of the manufacturer, effective 29/10/2024
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Cancellation or suspensionCancellation of the entry as the sponsor has refused or failed to comply with a condition to which the inclusion of the goods is subject (paragraph 30(2)(c) of the Act).
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Cancellation or suspensionCancellation of the entry due to the sponsor not providing sufficient information to substantiate compliance with the Essential Principles.
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Cancellation or suspensionCancellation of the entry due to the sponsor not providing sufficient information to substantiate compliance with the Essential Principles.
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Cancellation or suspensionCancellation of the entry due to incorrect classification of the device.
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Cancellation or suspensionCancellation from the ARTG under subsection 41GN(1)(b) of the Act
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Cancellation or suspensionCancellation from the ARTG under subsection 41GN(1) of the Act. Cancellation is limited to some medical devices of the kind and the ARTG is varied accordingly under section 41GO of the Act.
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Cancellation or suspensionCancellation from the ARTG under subsection 41GN(1) of the Act.
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Cancellation or suspensionCancellation from the ARTG under subsection 41GN(1) of the Act. Cancellation is limited to some medical devices of the kind and the ARTG is varied accordingly under section 41GO of the Act.
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Cancellation or suspensionCancellation from the ARTG under subsection 41GN(1) of the Act.
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Cancellation or suspensionCancellation from the ARTG under subsection 41GN(1) of the Act.
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Cancellation or suspensionCancellation from the ARTG under subsection 41GN(1) of the Act. Cancellation is limited to some medical devices of the kind and the ARTG is varied accordingly under section 41GO of the Act.
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Cancellation or suspensionCancellation from the ARTG under subsection 41GN(1) of the Act. Cancellation is limited to some medical devices of the kind and the ARTG is varied accordingly under section 41GO of the Act.
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Cancellation or suspensionCancellation from the ARTG under subsection 41GN(1) of the Act.
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Cancellation or suspensionCancellation from the ARTG under subsection 41GN(1) of the Act. Cancellation is limited to some medical devices of the kind and the ARTG is varied accordingly under section 41GO of the Act
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Cancellation or suspensionCancellation from the ARTG under subsection 41GN(1) of the Act. Cancellation is limited to some medical devices of the kind and the ARTG is varied accordingly under section 41GO of the Act.
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Cancellation or suspensionThe sponsor did not provide sufficient information to substantiate compliance with the Essential Principles, the sponsor failed to comply with a condition to which inclusion of the kind of device in the ARTG was subject, and the certifications made are incorrect, or are no longer correct, in a material particular.
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Cancellation or suspensionCancellation from the ARTG under subsection 41GN(1)(b) of the Act
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Cancellation or suspensionThe sponsor did not provide sufficient information to substantiate compliance with the Essential Principles, the sponsor failed to comply with a condition to which inclusion of the kind of device in the ARTG was subject.
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Cancellation or suspensionRegulatory action taken as it appears to the Secretary that the presentation of the goods is unacceptable (paragraph 30(2)(aa) of the Act).
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer, effective 31/07/2024
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer, effective 31/07/2024
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Cancellation or suspensionRegulatory action due to Voluntary revocation at the request of the manufacturer, effective 02/08/2024