PUBLIC COMMENT DRAFT MEDICAL DEVICE GUIDANCE DOCUMENT NOTIFICATION OF REFURBISHED MEDICAL DEVICE
DRAFT MEDICAL DEVICE GUIDANCE DOCUMENT
NOTIFICATION OF REFURBISHED MEDICAL DEVICE
This Guidance Document was prepared by the Medical Device Authority (MDA) to help the industry and healthcare professionals in their quest to comply with the Medical Device Act (Act 737) and the regulations under it.
This Guidance Document shall be read in conjunction with the current laws and regulations used in Malaysia, which include but not limited to the following-
a) Medical Device Act 2012 (Act 737);
b) Medical Device Regulations 2012;
This draft document is open for comment and feedback.
Please submit your feedback form to firstname.lastname@example.org before 28 February 2020