FINESTREAM S Plus PTA Balloon Dilatation Catheter - Indonesia BPOM Medical Device Registration

FINESTREAM S Plus PTA Balloon Dilatation Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501420075. The device is manufactured by GOODMAN CO., LTD. GOODMAN RESEARCH CENTER from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is MAKO DUA MEDIKAL.

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