KaiBiLi™ COVID-19 Antigen - Indonesia BPOM Medical Device Registration
KaiBiLi™ COVID-19 Antigen is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303127154. The device is manufactured by HANGZHOU GENESIS BIODETECTION AND BIOCONTROL CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SYNERGY INDOMITRA PRATAMA.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
China
Authorized Representative
PT. SYNERGY INDOMITRA PRATAMAAR Address
Jalan Tebet Timur Dalam 69B
Registration Date
Sep 20, 2022
Expiry Date
Jul 05, 2024
Product Type
Serological Reagents
Respiratory viral panel multiplex nucleic acid assay
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