ARIA TROPONIN I COMBO RAPID TEST - Indonesia BPOM Medical Device Registration
ARIA TROPONIN I COMBO RAPID TEST is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101027945. 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 HERMAN MEDTEK DIAGNOSTICS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BEIJING GENESEE BIOTECH INC.Country of Origin
China
Authorized Representative
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
Sep 20, 2021
Expiry Date
Jun 04, 2025
Product Type
Clinical Chemistry Test System
Creatine phosphokinase/creatine kinase or isoenzymes test system (card)
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