HEPA-B™ Rapid Test - Indonesia BPOM Medical Device Registration
HEPA-B™ Rapid Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30305220642. The device is manufactured by XIAMEN BOSON BIOTECH CO, LTD from China, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. ACCURATE INTAN MADYA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
XIAMEN BOSON BIOTECH CO, LTDCountry of Origin
China
Authorized Representative
PT. ACCURATE INTAN MADYAAR Address
KOMPLEK DUTA MERLIN, BLOK. F5 & F6, JL. GAJAH MADA NO. 3-5
Registration Date
Oct 01, 2024
Expiry Date
Sep 24, 2027
Product Type
Immunological Test System
Antimitochondrial antibody immunological test system.
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