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 DEVICEKF94 Respirator
ESTABLISHMENT NAMEDURIO PPE SDN. BHD.
ROLE OF ESTABLISHMENTMANUFACTURER
REGISTRATION NOGA6739823-137565
BRAND NAMEDurio
MEDICAL DEVICE CATEGORYSINGLE-USE DEVICES
DEVICE GROUPING TYPEFAMILY
DEVICE DESCRIPTIONKF94 Respirator is fluid-resistant, disposable, and tight-fitting devices that create a physical barrier between the mouth and nose of the wearer and the immediate environment.
DEVICE INTENDED PURPOSEDisposable device that covers the user’s nose and mouth and provides a physical barrier to droplets, fluids, bacteria and particulate materials.
VALIDITY DATE OF REGISTRATION28/06/2023 - 27/06/2028

LIST OF DEVICE

NONAME OF DEVICEIDENTIFIER
1Durio 904 KF94 Active Carbon Respirator 904 Active Carbon
2Durio 904 KF94 Neon Splash Respirator904 Neon Splash