KIFATEST Covid-19 Antigen - Indonesia BPOM Medical Device Registration
KIFATEST Covid-19 Antigen is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303220927. The device is manufactured by NANJING VAZYME MEDICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. KIMIA FARMA TBK..
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Risk Classification
Product Class
Kelas : 2
Manufacturer
NANJING VAZYME MEDICAL TECHNOLOGY CO., LTD.Country of Origin
China
Authorized Representative
PT. KIMIA FARMA TBK.AR Address
Jalan Veteran No.9
Registration Date
Dec 27, 2022
Expiry Date
Dec 26, 2023
Product Type
Serological Reagents
Respiratory viral panel multiplex nucleic acid assay
Invitro Diagnostics

