HEALGEN COVID-19 IgG/IgM Rapid Test Cassette (whole blood/serum/plasma) - Indonesia BPOM Medical Device Registration
HEALGEN COVID-19 IgG/IgM Rapid Test Cassette (whole blood/serum/plasma) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303023810. The device is manufactured by ZHEJIANG ORIENT GENE BIOTECH CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BINTANG MONO INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ZHEJIANG ORIENT GENE BIOTECH CO., LTD.Country of Origin
China
Authorized Representative
PT. BINTANG MONO INDONESIAAR Address
Perum Mahkota Simprug Blok A13 No. 9
Registration Date
May 25, 2021
Expiry Date
Mar 04, 2024
Product Type
Serological Reagents
Respiratory viral panel multiplex nucleic acid assay
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