PLANMECA ProOne - Indonesia BPOM Medical Device Registration

PLANMECA ProOne is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20601122868. The device is manufactured by PLANMECA LTD. from Finland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SATYA ABADI VISIMED.

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