ARIA TB IgG/IgM Combo Rapid Test - Indonesia BPOM Medical Device Registration
ARIA TB IgG/IgM Combo Rapid Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303027674. The device is manufactured by BEIJING GENESEE BIOTECH INC. from China, and is classified as Risk Class Kelas Resiko : C. 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
Nov 06, 2021
Expiry Date
Nov 05, 2024
Product Type
Serological Reagents
Mycobacterium tuberculosis immunofluorescent reagents.
Invitro Diagnostics
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ANSWER HBsAg Rapid Test
ANSWER Malaria Pf/Pan Ag Rapid Test
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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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