LANSIONBIO FT4 Test Kit (Dry Fluorescence Immunoassay) - Indonesia BPOM Medical Device Registration
LANSIONBIO FT4 Test Kit (Dry Fluorescence Immunoassay) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101323556. The device is manufactured by LANSION BIOTECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PRIORITA DIAN SARANA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LANSION BIOTECHNOLOGY CO., LTD.Country of Origin
China
Authorized Representative
PT. PRIORITA DIAN SARANAAR Address
Jl. RSI. Faisal Raya No. 06
Registration Date
Jul 26, 2023
Expiry Date
May 08, 2028
Product Type
Clinical Chemistry Test System
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