ARTIBEST Intra-articular Injection - Indonesia BPOM Medical Device Registration
ARTIBEST Intra-articular Injection is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31302220196. The device is manufactured by MAXIGEN BIOTECH INC. from Taiwan (China), and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. QUALTEK CONSULTANT JAKARTA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
MAXIGEN BIOTECH INC.Country of Origin
Taiwan (China)
Authorized Representative
PT. QUALTEK CONSULTANT JAKARTAAR Address
Icon Business Park Blok K No 6, BSD City, Kab Tangerang, Banten
Registration Date
Apr 27, 2022
Expiry Date
Nov 30, 2026
Product Type
Prosthetic Orthopedic Equipment
Intra articular fluid
Non Electromedic Sterile
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