VivaDiag™ Covid-19 IgM/IgG Rapid Test - Indonesia BPOM Medical Device Registration
VivaDiag™ Covid-19 IgM/IgG Rapid Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303023927. The device is manufactured by VIVACHECK BIOTECH (HANGZHOU) CO. LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. KIRANA JAYA LESTARI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
VIVACHECK BIOTECH (HANGZHOU) CO. LTDCountry of Origin
China
Authorized Representative
PT. KIRANA JAYA LESTARIAR Address
JL. TANAH ABANG II NO. 37
Registration Date
Jul 05, 2022
Expiry Date
Jun 06, 2024
Product Type
Serological Reagents
Respiratory viral panel multiplex nucleic acid assay
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