MANI Peeso Reamers - Indonesia BPOM Medical Device Registration

MANI Peeso Reamers is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10603814495. The device is manufactured by MANI, INC. KIYOHARA FACTORY. from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. FIXIPRIMA PERSADA.

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