CROSSROADS MG Guiding sheath - Indonesia BPOM Medical Device Registration

CROSSROADS MG Guiding sheath is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501420137. The device is manufactured by GOODMAN SEKI FACILITY 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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