FOKUS PCT (Procalcitonin) Rapid Quantitative Test (Immunofluorescence Assay) - Indonesia BPOM Medical Device Registration
FOKUS PCT (Procalcitonin) Rapid Quantitative Test (Immunofluorescence Assay) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303126297. The device is manufactured by SHENZHEN AEHEALTH TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FOCUS DIAGNOSTIC INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHENZHEN AEHEALTH TECHNOLOGY CO., LTDCountry of Origin
China
Authorized Representative
PT. FOCUS DIAGNOSTIC INDONESIAAR Address
Jl. Jatipadang Raya No.9A, RT.6/RW.4, Kelurahan Jatipadang, Kecamatan Pasar Minggu, Kota Jakarta Selatan, DKI Jakarta 12540
Registration Date
Jun 07, 2024
Expiry Date
Jun 06, 2027
Product Type
Serological Reagents
Procalcitonin test system
Invitro Diagnostics
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