ALLCHEK™ Dengue Duo NS1 & IgG/IgM Rapid Test - (WB/S/P) - Indonesia BPOM Medical Device Registration
ALLCHEK™ Dengue Duo NS1 & IgG/IgM Rapid Test - (WB/S/P) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303420242. The device is manufactured by HANGZHOU ALLTEST BIOTECH, CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is SAMUDERA INTI MEDISINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HANGZHOU ALLTEST BIOTECH, CO., LTD.Country of Origin
China
Authorized Representative
SAMUDERA INTI MEDISINDOAR Address
SAMUDERA INTI MEDISINDO
Registration Date
Jun 09, 2024
Expiry Date
Oct 04, 2028
Product Type
Serological Reagents
Dengue virus serological reagents
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