ARIA PSA Semi-Quantitative Rapid Test - Indonesia BPOM Medical Device Registration
ARIA PSA Semi-Quantitative Rapid Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20306220071. 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 HERMAN MEDTEK DIAGNOSTICS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BEIJING GENESEE BIOTECH, INCCountry 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
Jul 25, 2022
Expiry Date
Jun 04, 2025
Product Type
Tumor Antigen Immunologic Test System
Complexed Prostate Specific Antigen (CPSA) Immunological Test System
Invitro Diagnostics
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