ONCOPROBE HCV Antibody Rapid Test - Indonesia BPOM Medical Device Registration
ONCOPROBE HCV Antibody Rapid Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30305220651. The device is manufactured by FORMOSA BIOMEDICAL TECHNOLOGY CORP. from Taiwan (China), and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MAIN ONCOPROBE.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
FORMOSA BIOMEDICAL TECHNOLOGY CORP.Country of Origin
Taiwan (China)
Authorized Representative
PT. MAIN ONCOPROBEAR Address
APRT.ISTANA HARMONI LT.DASAR UNIT 1M, KOMP.HARMONI PLAZA JL.SURYOPRANOTO NO.2, PETOJO UTARA
Registration Date
Jan 24, 2023
Expiry Date
Dec 31, 2025
Product Type
Immunological Test System
Antinuclear antibody immunological test system.
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