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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 101 to 125
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Cancellation or suspensionThe sponsor failed to submit their annual report which is an automatic condition of inclusion under subsection 41FN(5A) of the Act.
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Cancellation or suspensionThe sponsor failed to submit their annual report which is an automatic condition of inclusion under subsection 41FN(5A) of the Act.
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Cancellation or suspensionThe sponsor failed to submit their annual report which is an automatic condition of inclusion under subsection 41FN(5A) of the Act.
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Cancellation or suspensionThe sponsor failed to submit their annual report which is an automatic condition of inclusion under subsection 41FN(5A) of the Act.
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Cancellation or suspensionThe sponsor failed to submit their annual report which is an automatic condition of inclusion under subsection 41FN(5A) of the Act.
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Cancellation or suspensionThe sponsor failed to submit their annual report which is an automatic condition of inclusion under subsection 41FN(5A) of the Act.
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Cancellation or suspensionThe sponsor failed to submit their annual report which is an automatic condition of inclusion under subsection 41FN(5A) of the Act.
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Cancellation or suspensionThe sponsor failed to submit their annual report which is an automatic condition of inclusion under subsection 41FN(5A) of the Act.
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Cancellation or suspensionThe sponsor failed to submit their annual report which is an automatic condition of inclusion under subsection 41FN(5A) of the Act.
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Cancellation or suspensionThe sponsor failed to submit their annual report which is an automatic condition of inclusion under subsection 41FN(5A) of the Act.
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Cancellation or suspensionWe have cancelled Philips Electronics Australia Ltd, Portable ventilator, electric/47083: Trilogy EV300, INTL-Model IN2200X15B - Under subsection 41GK(1)
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Cancellation or suspensionWe have cancelled Philips Electronics Australia Ltd - Portable ventilator, electric/47083: Trilogy Evo, O2, International - Model IN2100X15B under s41 GK(1) of the Act
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Cancellation or suspensionComplementary medicine cancellation from the ARTG, under subsection 30(2) of the Act.
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Cancellation or suspensionRegulatory action due to , effective 18/04/2024
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Cancellation or suspensionRegulatory action due to , effective 3/04/2024
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Cancellation or suspensionWe have cancelled Evolve Therapeutic Aesthetic Supplies Pty Ltd - Hair-removal diode laser system under subsection 41GM(2) of the Act
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Cancellation or suspensionWe have cancelled ND:YAG - Dermatological Nd:YAG/Frequency-doubled Nd:YAG laser system under subsection 41GM(2) of the Act
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Cancellation or suspensionWe have cancelled Soma Lasers Australia - Hair-removal diode laser system under subsection 41GM(2) of the Act
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Cancellation or suspensionThe device is being cancelled due to failure to comply with an automatic condition of inclusion under subsection 41FN(5A) of the Act, effective from 25 March 2024.
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Cancellation or suspensionThe device is being cancelled due to failure to comply with an automatic condition of inclusion under s. 41FN(5A) of the Act, effective from 25 March 2024.
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Cancellation or suspensionThe device is being cancelled due to failure to comply with an automatic condition of inclusion under subsection 41FN(5A) of the Act, effective from 25 March 2024.
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Cancellation or suspensionThe device is being cancelled due to failure to comply with an automatic condition of inclusion under subsection 41FN(5A) of the Act, effective from 25 March 2024.
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Cancellation or suspensionThe device is being cancelled due to failure to comply with an automatic condition of inclusion under subsection 41FN(5A) of the Act, effective from 25 March 2024.
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Cancellation or suspensionThe device is being cancelled due to failure to comply with an automatic condition of inclusion under subsection 41FN(5A) of the Act, effective from 25 March 2024.
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Cancellation or suspensionThe device is being cancelled due to failure to comply with an automatic condition of inclusion under subsection 41FN(5A) of the Act, effective from 25 March 2024.