The Supplementary Information Sheet for Medical Devices Procured by the Hospital Authority (HA)(MD111) on this page are relevant to device(s) which had been procured by the Hospital Authority. When submitting a medical device listing application, the applicant should include the duly completed Supplementary Information Sheet.
Applicants are advised to take reference to documents issued under the Medical Device Administrative Control System when completing their medical device listing application.
Medical Device Division has introduced a new Medical Device Information System (MDIS) on 2 April 2024, which will offer a one-stop e-service for the industry to submit online applications for listing of medical devices (MDs) and traders under the Medical Device Administrative Control System (MDACS), as well as to report safety alerts and adverse events related to MDs. Please refer to the Medical Device Information System (MDIS) Theme page for details.
Only submissions with duly completed application forms and required documents will be processed. Materials provided with any submission will not be returned.