This facility is provided to enable any interested parties to search for Registered Medical Device, Registered CAB, Licensed Establishments under Section 5, 10, 15 of Medical Device Act 2012 (Act 737) respectively and Notified Medical Device under Medical Device (Exemption) Order 2016. Any party who wishes to know whether an establishment who is dealing with medical device has been licensed under Act 737 may search the establishment by inserting the establishment name or license number in the searching field below.


DEVICE DETAILS

NAME OF DEVICEPROCEDURE FACE MASK
ESTABLISHMENT NAMEMUN GLOBAL SDN BHD
REGISTRATION NOGA7483422-106656
BRAND NAMEPRIMEON
DEVICE GROUPING TYPESINGLE
DEVICE DESCRIPTIONA single-use procedure mask is a loose-fitting, non-sterile device made from non-woven material that creates a physical barrier between the mouth and nose of the wearer and potential contaminants in the immediate environment.
DEVICE INTENDED PURPOSEIt is intended to prevent the transmission of microorganisms, body fluids and particulate material in healthcare setting for everyday use.
VALIDITY DATE OF REGISTRATION26/10/2022 - 25/10/2027

LIST OF DEVICE

NONAME OF DEVICEDEVICE IDENTIFIER
1PROCEDURE FACE MASKFPM21UN