APERTA NSE Coronary Dilation Catheter - Indonesia BPOM Medical Device Registration

APERTA NSE Coronary Dilation Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501320879. The device is manufactured by GOODMAN CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MAKO TWO MEDICAL.

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