AIM Rapid Test Typhoid-F - Indonesia BPOM Medical Device Registration
AIM Rapid Test Typhoid-F is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303520048. The device is manufactured by HANGZHOU ALLTEST BIOTECH CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ACCURATE INTAN MADYA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HANGZHOU ALLTEST BIOTECH CO., LTD.Country of Origin
China
Authorized Representative
PT. ACCURATE INTAN MADYAAR Address
KOMPLEK DUTA MERLIN, BLOK. F5 & F6, JL. GAJAH MADA NO. 3-5
Registration Date
Jan 17, 2025
Expiry Date
Jan 16, 2028
Product Type
Serological Reagents
Salmonella spp. serological reagents.
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