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 DEVICENEUTROVIS KF94 KOREAN PREMIUM FACE RESPIRATOR
ESTABLISHMENT NAMENEUTROVIS SDN BHD
REGISTRATION NOGA3758923-116456
BRAND NAMENEUTROVIS
DEVICE GROUPING TYPEFAMILY
DEVICE DESCRIPTIONNeutrovis KF94 Korean Premium Face Respirator is designed to limit unfiltered air entry with the flaps staying flush against your face and provides a secure seal and double protection from all sides of the face mask. The 2 layers of inner melt-blown fabric and its innovative 3D design allow for more space between your mouth and the face mask and reduced the risk of the wearer readjusting their face mask
DEVICE INTENDED PURPOSENeutrovis KF94 Korean Premium Face Respirator with >=98% PFE and >=98% BFE able to filter out bacteria, pollution, pollen and dust particles from our surroundings
VALIDITY DATE OF REGISTRATION21/01/2023 - 20/01/2028

LIST OF DEVICE

NONAME OF DEVICEIDENTIFIER
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