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.


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DEVICE DETAILS

NAME OF DEVICESURGICAL FACE MASK
ESTABLISHMENT NAMEMUN GLOBAL SDN BHD
REGISTRATION NOGA8685223-145098
BRAND NAMEPRIMEON
DEVICE GROUPING TYPEFAMILY
DEVICE DESCRIPTIONA single-use surgical 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 surgical tasks.
VALIDITY DATE OF REGISTRATION20/08/2023 - 19/08/2028

LIST OF DEVICE

NONAME OF DEVICEIDENTIFIER
1MUN PrimeOn Artemis Surgical Face Mask FPM20UN
2MUN PrimeOn Artemis Surgical Face Mask FPM23UN
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