Cardioplegia coronary perfusion cannula (Revocation of suspension)
Product name
Cardioplegia coronary perfusion cannula
Sponsor
ARTG
155615
Date action takes effect
Lapse date
Compliance action
Medical device suspension
Type of action
Revocation of suspension
Grounds for regulatory action
Grounds for extension of the suspension: The ARTG entries were suspended by the Secretary in accordance with paragraph 41GA(1)(b) of the Act. The reason for suspension was failure to comply with the conditions of inclusion related to the availability of the information demonstrating the application of the appropriate conformity assessment procedure.
The suspension was revoked by the Secretary as the grounds for cancelling this kind of device from the ARTG no longer apply.