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 DEVICENEUTROVIS KN95 FACE RESPIRATOR
ESTABLISHMENT NAMENEUTROVIS SDN BHD
ROLE OF ESTABLISHMENTMANUFACTURER
REGISTRATION NOGA7413323-116670
BRAND NAMENEUTROVIS
MEDICAL DEVICE CATEGORYSINGLE-USE DEVICES
DEVICE GROUPING TYPEFAMILY
DEVICE DESCRIPTIONNeutrovis KN95 Face Respirator made with 2 layers of inner melt-blown fabric with >=98% BFE & >= 98% PFE to able effectively filter viable and nonviable particles such as bacteria, pollen and dust particles form our surrounding
DEVICE INTENDED PURPOSENeutrovis KN95 Face Respirator is made to limit unfiltered air entry to provide better protection against airborne particles. The tight fit around the bridge of your nose and sides of your cheeks directs air to pass through the filter so that you're safe to breathe
VALIDITY DATE OF REGISTRATION24/01/2023 - 23/01/2028

LIST OF DEVICE

NONAME OF DEVICEIDENTIFIER
1Neutrovis KN95 Face RespiratorNTV03
2Neutrovis KN95 Face RespiratorNTV134
3Neutrovis KN95 Face RespiratorNTV135
4Neutrovis KN95 Face RespiratorNTV136
5Neutrovis KN95 Face RespiratorNTV137
6Neutrovis KN95 Face RespiratorNTV249
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