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 DEVICEIONSPEC Spectacles
ESTABLISHMENT NAMEEPORT SDN BHD
ROLE OF ESTABLISHMENTAUTHORIZED REPRESENTATIVE
REGISTRATION NOGA10865523-148219
BRAND NAMEIONSPEC
MEDICAL DEVICE CATEGORYOPTHALMIC AND OPTICAL DEVICES
DEVICE GROUPING TYPEFAMILY
DEVICE DESCRIPTIONIonSpec is manufactured in compliance to QMS: ISO 13485 using nano technology and patented materials. Used accordingly it will help to filter UV light and improve common eye problem.
DEVICE INTENDED PURPOSEIonSpec is manufactured in compliance to QMS: ISO 13485 using nano technology and patented materials. Used accordingly it will help to filter UV light and improve common eye problem.
VALIDITY DATE OF REGISTRATION20/09/2023 - 19/09/2028

LIST OF DEVICE

NONAME OF DEVICEIDENTIFIER
1IONSPEC TR90 M001-M999
2IONSPEC ULTEM M001-M999
3IONSPEC TITANIUMM001-M999
4IONSPEC HAND CRAVED M001-M999
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