ARIA Syphilis Ab Rapid Test - Indonesia BPOM Medical Device Registration
ARIA Syphilis Ab Rapid Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303027252. 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 10, 2021
Expiry Date
Jun 04, 2025
Product Type
Serological Reagents
Treponema pallidum treponemal test reagents.
Invitro Diagnostics
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ARIA Leptospira IgG/IgM Combo Rapid Test
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