FOKUS Febrile Antigen H-B Paratyphi - Indonesia BPOM Medical Device Registration
FOKUS Febrile Antigen H-B Paratyphi is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303220236. The device is manufactured by PULSE SCIENTIFIC INC. from Canada, 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
PULSE SCIENTIFIC INC.Country of Origin
Canada
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
Jan 04, 2025
Expiry Date
Jan 02, 2028
Product Type
Serological Reagents
Salmonella spp. serological reagents.
Invitro Diagnostics
FOKUS Febrile Antigen H-A Paratyphi
FOKUS Febrile Antigen H-C Paratyphi
FOKUS Febrile Antigen H Typhi
FOKUS Febrile Antigen O-A Paratyphi
FOKUS Febrile Antigen O-B Paratyphi
FOKUS Febrile Antigen O-C Paratyphi
FOCUS Antistreptolysin-O (ASO) Latex Test
FOKUS RPR Antigen Test
FOKUS RF Latex
FOKUS CRP Latex Test
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