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 PREMIUM MEDICAL FACE MASK
ESTABLISHMENT NAMEROCKY SCIENTIFIC INSTRUMENTATION
REGISTRATION NOGA2211920-50702
BRAND NAMEFRONTIFIE
DEVICE GROUPING TYPEFAMILY
DEVICE DESCRIPTIONTHE PRODUCT IS MADE OF MELT-BLOWN FABRIC WITH BFE (BACTERIAL FILTRATION EFFICIENCY) >98% AND PFE ( PARTICLE FILTRATION EFFICIENCY) >96%, WHICH IS USED TO BLOCK LIVE BACTERIA (VIABLE PARTICLES) FROM 1 TO 5 MICRON AND MICRO PARTICLES (NONVIABLE PARTICLES) FROM 0.1 MICRON TO 1 MICRON
DEVICE INTENDED PURPOSEto provide a barrier and to protect the patient and hospital staff or doctors from direct transmission of infective agents, blood,splash,viruses, suitable to be used in a medical, surgical,dental and public
VALIDITY DATE OF REGISTRATION17/12/2020 - 16/12/2025

LIST OF DEVICE

NONAME OF DEVICEIDENTIFIER
1FRONTIFIE PREMIUM MEDICAL FACE MASKOTR003
2FRONTIFIE PREMIUM MEDICAL FACE MASKOTR005
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