AIM Dengue Tripleline Rapid Test - Indonesia BPOM Medical Device Registration
AIM Dengue Tripleline Rapid Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303120198. The device is manufactured by XIAMEN BOSON BIOTECH CO, LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ACCURATE INTAN MADYA.
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Risk Classification
Product Class
Kelas : 2
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
Sep 02, 2023
Expiry Date
Jan 08, 2025
Product Type
Serological Reagents
Dengue virus serological reagents
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