ARIA Typhoid IgG/IgM Rapid Test - Indonesia BPOM Medical Device Registration
ARIA Typhoid IgG/IgM Rapid Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303027946. The device is manufactured by BEIJING GENESEE BIOTECH INC. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. HERMAN MEDTEK DIAGNOSTICS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BEIJING GENESEE BIOTECH INC.Country of Origin
China
Authorized Representative
PT. HERMAN MEDTEK DIAGNOSTICSAR Address
Jl. Lingkar Luar Barat, Puri Kembangan, Komplek Rukan Puri Mansion Blok A No.16 Kel.Kembangan Selatan Kec.Kembangan, Kota Jakarta Barat, DKI Jakarta
Registration Date
Dec 17, 2020
Expiry Date
May 18, 2025
Product Type
Serological Reagents
Salmonella spp. serological reagents.
Invitro Diagnostics
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ANSWER Leptospira IgG/IgM Combo Rapid Test Cassette
ANSWER HCV Ab Plus Rapid Test
ARIA Chlamydia Ag Rapid Test
ARIA Syphilis Ab Rapid Test
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