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 DEVICEDurio Surgical Respirator
ESTABLISHMENT NAMEDURIO PPE SDN BHD
ROLE OF ESTABLISHMENTMANUFACTURER
REGISTRATION NOGA6249522-87915
BRAND NAMEDurio
MEDICAL DEVICE CATEGORYSINGLE-USE DEVICES
DEVICE GROUPING TYPEFAMILY
DEVICE DESCRIPTIONRespirator is fluid-resistant, disposable, and fitting devices that create a physical barrier between the mouth and nose of the wearer and the immediate environment.
DEVICE INTENDED PURPOSEUsed inside the operating room or within other sterile procedure areas to protect the patient environment from contamination.
VALIDITY DATE OF REGISTRATION16/03/2022 - 15/03/2027

LIST OF DEVICE

NONAME OF DEVICEIDENTIFIER
1KN95 3D Foldable Respirator901
2N95 Particulate Respirator902
3KN95 Respirator903
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