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 DEVICEGentle
ESTABLISHMENT NAMEPFLEGE MEDICAL SUPPLIES SDN. BHD.
ROLE OF ESTABLISHMENTMANUFACTURER
REGISTRATION NOGA6912921-59772
BRAND NAMEPROFIX
MEDICAL DEVICE CATEGORYSINGLE-USE DEVICES
DEVICE GROUPING TYPESINGLE
DEVICE DESCRIPTIONPROFIX Gentle is adhesive plaster with dimension 7.2 x 1.9 cm.
DEVICE INTENDED PURPOSEPROFIX Gentle is intended to be used for hypoallergenic and sensitive skin, extraction of exudes, compression or protecting wounds and wound surfaces.
VALIDITY DATE OF REGISTRATION20/04/2021 - 19/04/2026

LIST OF DEVICE

NONAME OF DEVICEDEVICE IDENTIFIER
1GentleGE30
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