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 DEVICEKN 95/FFP2 MEDICAL FACE MASK
ESTABLISHMENT NAMECARELINE MANUFACTURING SDN BHD
REGISTRATION NOGA4956722-99175
BRAND NAMECARELINE
DEVICE GROUPING TYPESINGLE
DEVICE DESCRIPTIONKN 95/FFP2 MEDICAL Face Mask is intended for single use and suitable for general use, blocking the exhalation and inhalation of pathogens and airborne liquid droplets expelled by coughing, sneezing and respiration.
DEVICE INTENDED PURPOSEThe Careline KN 95/FFP2 Medical Face Mask effectively isolates air pollution, bacteria ,particle dust and pollen. It blocks the exhalation and inhalation of pathogens and airborne liquid droplets expelled by coughing, sneezing and respiration.
VALIDITY DATE OF REGISTRATION01/08/2022 - 31/07/2027

LIST OF DEVICE

NONAME OF DEVICEDEVICE IDENTIFIER
1KN 95/FFP2 MEDICAL FACE MASKKN95/FFP2-MEDICAL-CARELINE
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