SONOLITH i-Move - Indonesia BPOM Medical Device Registration

SONOLITH i-Move is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805012387. The device is manufactured by EDAP TMS FRANCE S.A. from France, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. INDOSOPHA SAKTI.

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