Use the filters below to narrow your search.
Filter results
You can narrow down the results using the filters.
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.
Results for
"[search-keyword]"
Search
1780 result(s) found, displaying 801 to 825
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 19/03/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 19/03/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 19/03/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 19/03/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 19/03/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 19/03/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 19/03/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 19/03/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 19/03/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 19/03/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 19/03/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 19/03/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 19/03/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 05/03/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 05/03/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 05/03/2021
-
Cancellation or suspensionRegulatory action due to Failure to comply with s41JA within a further 10 days, effective 05/03/2021
-
Cancellation or suspensionRegulatory action due to Failure to comply with s41JA within a further 10 days, effective 05/03/2021
-
Cancellation or suspensionRegulatory action due to Failure to comply with s41JA within a further 10 days, effective 05/03/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 04/03/2021
-
Cancellation or suspensionRegulatory action due to Failure to comply with s41JA within a further 10 days, poor device safety and incorrect certification, effective 04/03/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 01/03/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 01/03/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 24/02/2021
-
Cancellation or suspensionRegulatory action due to Non response to a s41JA, effective 22/02/2021