K-MOD PS - Indonesia BPOM Medical Device Registration

K-MOD PS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302915578. The device is manufactured by GRUPPO BIOIMPIANTI S.R.L from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. INDO PREMIER ORTHO.

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