FOCUS S. Paratyphi 'AH' Antigen - Indonesia BPOM Medical Device Registration
FOCUS S. Paratyphi 'AH' Antigen is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303025941. The device is manufactured by TULIP DIAGNOSTICS PVT., LTD. from India, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FOCUS DIAGNOSTIC INDONESIA.
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FOKUS S. Paratyphi 'AH' Antigen
Risk Classification
Product Class
Kelas : 2
Manufacturer
TULIP DIAGNOSTICS PVT., LTD.Country of Origin
India
Authorized Representative
PT. FOCUS DIAGNOSTIC INDONESIAAR Address
18 Office Park, Tower A, Jl. TB Simatupang No.18 MZ Floor, Unit D1-A/89, Kelurahan Kebagusan
Registration Date
Apr 05, 2022
Expiry Date
Mar 01, 2025
Product Type
Serological Reagents
Salmonella spp. serological reagents.
Invitro Diagnostics
BAV Widal S. Typhi O
FOKUS Widal Negative Control
FOCUS 6 PRAYER
FOCUS Widal Positive Control
FOCUS S. Typhi 'H' Antigen
FOCUS S. Typhi 'O' Antigen
FOKUS S. Paratyphi 'AO' Antigen
FOKUS S. Paratyphi 'CH' Antigen
FOKUS S. Paratyphi 'CO' Antigen
FOKUS S. Paratyphi 'BO' Antigen
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