AFIAS PSA - Indonesia BPOM Medical Device Registration

AFIAS PSA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20306717046. The device is manufactured by BODITECH WITH INC. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is TRIPATRIA MAINSTAY MEDIKA.

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