RELIAFIX PEEK Interference Screw - Indonesia BPOM Medical Device Registration
RELIAFIX PEEK Interference Screw is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302123938. The device is manufactured by HANGZHOU REJOIN MASTIN MEDICAL DEVICE CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ALLVAMED NUVACON ADIGANA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HANGZHOU REJOIN MASTIN MEDICAL DEVICE CO., LTD.Country of Origin
China
Authorized Representative
PT. ALLVAMED NUVACON ADIGANAAR Address
BELLEZA BSA JL. LETJEN SOEPENO
Registration Date
Jul 05, 2021
Expiry Date
Mar 11, 2026
Product Type
Prosthetic Orthopedic Equipment
Smooth or threaded metallic bone fixation fastener.
Non Electromedic Sterile
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