PLANMECA ProMax 3D Mid - Indonesia BPOM Medical Device Registration

PLANMECA ProMax 3D Mid is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20601420019. The device is manufactured by PLANMECA LTD. from Finland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is SATYA ABADI VISIMED.

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