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 DEVICEFRONTIFIE 4-PLY HEADLOOP SURGICAL FACE MASK
ESTABLISHMENT NAMENEUTROVIS SDN BHD
REGISTRATION NOGA3627623-132592
BRAND NAMEFRONTIFIE
DEVICE GROUPING TYPEFAMILY
DEVICE DESCRIPTIONThis single use surgical face mask with BFE >= 98% and PFE >=98% is made from premium medical grade melt-blown filter fabric that will protect you from germs, bacteria and viruses. The soft, non-woven, inner material of the mask provides better comfort and reduced irritation. It is able to filter out live bacteria (viable particles) from 5 to 1 micron and micro particles (nonviable particles) from 1 to 0.1 micron
DEVICE INTENDED PURPOSE4 PLY DISPOSABLE MEDICAL AND SURGICAL FACE MASK IS A NON-WOVEN MATERIAL THAT OFFERS FILTRATION-EFFICIENT, FLUID-RESISTANT, SUPERIOR COMFORT AND BREATHABILITY TO HELP REDUCE WEARER TO EXPOSURE OF POTENTIALLY INFECTIOUS PARTICLES, BLOOD AND BODY FLUIDS . IT IS DESIGNED TO BE USED IN HOSPITAL ESPECIALLY IN OPERATING THEATER AND CLEAN ROOM ENVIRONMENT.
VALIDITY DATE OF REGISTRATION26/05/2023 - 25/05/2028

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