ANSWER Dengue IgG/IgM Combo Rapid Test - Indonesia BPOM Medical Device Registration
ANSWER Dengue IgG/IgM Combo Rapid Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303123793. The device is manufactured by BEIJING GENEESE BIOTECH. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. EXXEL MAIN.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BEIJING GENEESE BIOTECH.Country of Origin
China
Authorized Representative
PT. EXXEL MAINAR Address
JALAN RAJAWALI SELATAN.RUKO MULTI GUNA KEMAYORAN BLOK.6N.JAKARTA UTARA
Registration Date
Oct 25, 2023
Expiry Date
Sep 14, 2025
Product Type
Serological Reagents
Dengue virus serological reagents
Invitro Diagnostics
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