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 DEVICEMEDICAL FACE MASK
ESTABLISHMENT NAMECARELINE MANUFACTURING SDN BHD
REGISTRATION NOGA7113021-62086
BRAND NAMECARELINE
DEVICE GROUPING TYPESINGLE
DEVICE DESCRIPTIONSingle use 3 ply non sterile medical ( TypeIIR) complying to ASTM 2100 and EN14683.
DEVICE INTENDED PURPOSECareline 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.
VALIDITY DATE OF REGISTRATION24/05/2021 - 23/05/2026

LIST OF DEVICE

NONAME OF DEVICEDEVICE IDENTIFIER
1MEDICAL FACE MASK050521-SO1
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