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 DEVICEEar-loop Face Mask (3ply)
ESTABLISHMENT NAMEMEDIMEX SDN BHD
ROLE OF ESTABLISHMENTAUTHORIZED REPRESENTATIVE
REGISTRATION NOGA8648422-88205
BRAND NAMEXecare
MEDICAL DEVICE CATEGORYSINGLE-USE DEVICES
DEVICE GROUPING TYPEFAMILY
DEVICE DESCRIPTION3 ply surgical face mask with earloop, latex free, antifog and hypoallergic
DEVICE INTENDED PURPOSEUsed to create physical barrier for mouth and nose of wearer and potential contaminants in the environment.
VALIDITY DATE OF REGISTRATION18/03/2022 - 17/03/2027

LIST OF DEVICE

NONAME OF DEVICEIDENTIFIER
1Ear-loop Face Mask (3ply) AdultMXFMS01
2Ear-loop Face Mask (3 ply) ChildMXFMS02
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