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 DEVICEREJURAN HB PLUS
ESTABLISHMENT NAMEELOGIO ASIA PACIFIC SDN BHD
ROLE OF ESTABLISHMENTAUTHORIZED REPRESENTATIVE
REGISTRATION NOGD11766525-217431
BRAND NAMEREJURAN
MEDICAL DEVICE CATEGORYMD 0102 - Non-active devices for injection, infusion, transfusion and dialysis
DEVICE GROUPING TYPESINGLE
DEVICE DESCRIPTIONREJURAN® HB plus is a gel for intradermal implants consisting of Sodium Polynucleotide 1 %, Sodium Hyaluronate 1 % and Lidocaine Hydrochloride Hydrate 0.3 %, highly purified, long chain molecule from natural origin. It is pre-filled in syringe with up to 1.0 mL, sterile, and for single use only.
DEVICE INTENDED PURPOSESodium Hyaluronate and Sodium Polynucleotide are injected under the skin to temporarily improve the crow’s feet of adults through physical recovery.
VALIDITY DATE OF REGISTRATION25/11/2025 - 24/11/2030

LIST OF DEVICE

NONAME OF DEVICEDEVICE IDENTIFIER
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