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 DEVICESurgical Face Mask
ESTABLISHMENT NAMECREATIVE CONTRACT (M) SDN BHD
REGISTRATION NOGA9892321-55677
BRAND NAMEBreeze
DEVICE GROUPING TYPESINGLE
DEVICE DESCRIPTION3-ply Super Soft PP Non-Woven - Latex-Free & Hypoallergenic - Bacterial Filtration Efficiency > 99% - Particle Filtration Efficiency 0.1%u03BC > 98% - Fluid Resistant
DEVICE INTENDED PURPOSEmedical device covering the mouth, nose and chin ensuring a barrier that limits the transition of an infective agent between the hospital staff and the patient
VALIDITY DATE OF REGISTRATION23/02/2021 - 22/02/2026

LIST OF DEVICE

NONAME OF DEVICEDEVICE IDENTIFIER
1Surgical Face MaskBreeze
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