LIFOTRONIC fT4 Test (FIA) - Indonesia BPOM Medical Device Registration
LIFOTRONIC fT4 Test (FIA) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101420678. The device is manufactured by SHENZHEN LIFOTRONIC TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. LIFOTRONIC TECHNOLOGY INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHENZHEN LIFOTRONIC TECHNOLOGY CO., LTD.Country of Origin
China
Authorized Representative
PT. LIFOTRONIC TECHNOLOGY INDONESIAAR Address
Ruko South Goldfinch Blok SGA No. 17, Jl. Spring Boulevard, Kode Pos 15322, Kel. Cihuni, Kec. Pagedangan, Kab. Tangerang, Provinsi Banten
Registration Date
Apr 16, 2024
Expiry Date
Mar 13, 2028
Product Type
Clinical Chemistry Test System
Free thyroxine test system (kit & cair)
Invitro Diagnostics
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LIFOTRONIC Creatine Kinase MB (Electrochemiluminescence Immunoassay)
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LIFOTRONIC Ferritin (Electrochemiluminescence lmmunoassay)
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