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 DEVICEPROCEDURAL EARLOOP FACE MASKS
ESTABLISHMENT NAMECANTEL MEDICAL (MALAYSIA) SDN. BHD.
REGISTRATION NOGMD9934417116A
BRAND NAMEPROCEDURAL
DEVICE GROUPING TYPEFAMILY
DEVICE DESCRIPTIONASTM Level 2 face mask with fluid resistant outer layer, soft tissue inner layer and extra long nose piece.
DEVICE INTENDED PURPOSECrosstex surgical masks are intended for the use in infection control practices to minimuze contamination caused by inhaled and exhaled microorganisms and reduce the potential exposure of the wearer to blood and body fluids.
VALIDITY DATE OF REGISTRATION20/09/2021 - 19/09/2026

LIST OF DEVICE

NONAME OF DEVICEIDENTIFIER
1Procedural - EarloopGCPBL100
2Procedural - EarloopGCPYE
3Procedural - EarloopGCPPK
4Procedural - EarloopGCPLV
5Procedural - EarloopGCPBL
6Procedural Earloop w/SecureFit® TechnologyGCPBLSF
7Procedural Earloop w/SecureFit® TechnologyGCPLVSF
8Procedural Earloop w/SecureFit® TechnologyGCPPKSF
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