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.


DEVICE DETAILS

NAME OF DEVICEISOFLUID FACE MASKS
ESTABLISHMENT NAMECANTEL MEDICAL (MALAYSIA) SDN. BHD.
REGISTRATION NOGMD8937711916A
BRAND NAMEISOFLUID
DEVICE GROUPING TYPEFAMILY
DEVICE DESCRIPTIONASTM Level 1 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 minimize contamination caused by inhaled and exhaled microorganisms and reduce the potential exposure of the wearer to blood and body fluids.
VALIDITY DATE OF REGISTRATION14/09/2021 - 13/09/2026

LIST OF DEVICE

NONAME OF DEVICEIDENTIFIER
1Isofluid® - EarloopGCIBL
2Isofluid® - EarloopGCIGR
3Isofluid® - EarloopGCILV
4Isofluid® - EarloopGCIPK
5Isofluid® - EarloopGCISA
6Isofluid® - EarloopGCITE
7Isofluid® - EarloopGCITZ
8Isofluid® - EarloopGCITQ
9Isofluid® - EarloopGCIBL100
10Isofluid® Plus - EarloopGPLUSBL
11Isofluid® Plus - EarloopGPLUSKA
12Isofluid® Plus - EarloopGPLUSPK
13Isofluid® Plus Pure w/Secure-Fit® TechnologyGPLUSWHSF
14Isofluid® Plus Pure w/Secure-Fit® TechnologyGCIBLSF
15Isofluid® Plus Pure w/Secure-Fit® TechnologyGCILVSF
16Isofluid® Plus Pure w/Secure-Fit® TechnologyGCIPKSF