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 DEVICEWRIST BLOOD PRESSURE MONITOR
ESTABLISHMENT NAMEHUAWEI TECHNOLOGIES (MALAYSIA) SDN BHD
REGISTRATION NOGB2822524-166644
BRAND NAMEHUAWEI
DEVICE GROUPING TYPEFAMILY
DEVICE DESCRIPTIONThe Wrist Blood Pressure Monitor manufactured by Huawei Device Co., Ltd. (hereafter referred to as Huawei) is a reusable, active, non-sterile, non-invasive and non-implantable device for measuring adults’ blood pressure and pulse rate. It is a home-use device prohibited from use in MRI (magnetic resonance imaging) environment.
DEVICE INTENDED PURPOSEThe Wrist Blood Pressure Monitor is a digital self-monitor intended for use in measuring blood pressure and pulse rate in adult patient population with wrist circumference ranging from 13.0 cm to 20.0 cm (5.12–7.87 inches).
VALIDITY DATE OF REGISTRATION19/03/2024 - 18/03/2029

LIST OF DEVICE

NONAME OF DEVICEIDENTIFIER
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