WEMED Rapid Test for Antibody to Syphilis (Colloidal Gold Device) - Indonesia BPOM Medical Device Registration
WEMED Rapid Test for Antibody to Syphilis (Colloidal Gold Device) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303910841. The device is manufactured by BEIJING WANTAI BIOLOGICAL PHARMACY ENTERPRISE CO.,LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. WEGO MEDIKA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
China
Authorized Representative
PT. WEGO MEDIKA INDONESIAAR Address
Jl. Tanah Abang II No.67 Kel. Petojo Selatan, Kec. Gambir, Jakarta Pusat
Registration Date
Jul 06, 2022
Expiry Date
Jun 30, 2024
Product Type
Serological Reagents
Treponema pallidum treponemal test reagents.
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