WEMED Rapid Test for IgM Antibody to Hepatitis A Virus (Colloidal Gold Device) - Indonesia BPOM Medical Device Registration
WEMED Rapid Test for IgM Antibody to Hepatitis A Virus (Colloidal Gold Device) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303918240. The device is manufactured by BEIJING WANTAI BIOLOGICAL PHARMACY ENTERPRISE CO.,LTD. from China, and is classified as Risk Class Kelas Resiko : B. 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
Apr 11, 2022
Expiry Date
Jun 30, 2024
Product Type
Serological Reagents
Hepatitis A virus (HAV) serological assays.
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