AFIAS COVID-19 From - Indonesia BPOM Medical Device Registration

AFIAS COVID-19 From is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303027004. The device is manufactured by BODITECH WITH INC. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is TRIPATRIA MAINSTAY MEDIKA.

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