ALL-TEST™ Dengue Rapid Test Cassette (Whole Blood/Serum/Plasma) - Indonesia BPOM Medical Device Registration
ALL-TEST™ Dengue Rapid Test Cassette (Whole Blood/Serum/Plasma) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303912713. 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 MITRA BAHAGIA CITRA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HANGZHOU ALLTEST BIOTECH CO., LTD.Country of Origin
China
Authorized Representative
MITRA BAHAGIA CITRA MEDIKAAR Address
Jl. Raya Kalirungkut 27 Blok C-63
Registration Date
Jun 13, 2023
Expiry Date
Oct 09, 2027
Product Type
Serological Reagents
Plasmodium species antigen detection assays
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