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 DEVICECALLIE FFP2 NR D PARTICULATE RESPIRATOR SURGICAL KN95
ESTABLISHMENT NAMEPECCA LEATHER SDN BHD
ROLE OF ESTABLISHMENTMANUFACTURER
REGISTRATION NOGA7853721-59028
BRAND NAMECALLIE
MEDICAL DEVICE CATEGORYSINGLE-USE DEVICES
DEVICE GROUPING TYPESINGLE
DEVICE DESCRIPTIONConsists of 4 layers for excellent filtration efficiency, pre-shaped nose cushion and contoured facial seal, soft and elastic ear-tie for easy and comfort wear.
DEVICE INTENDED PURPOSEFiltering facemask respirator for surgical, medical and general use.
VALIDITY DATE OF REGISTRATION08/04/2021 - 07/04/2026

LIST OF DEVICE

NONAME OF DEVICEDEVICE IDENTIFIER
1CALLIE FFP2 NR D PARTICULATE RESPIRATOR SURGICAL KN95CL-201