TRAXCESS Guidewire - Indonesia BPOM Medical Device Registration

TRAXCESS Guidewire is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501911239. The device is manufactured by ASHITAKA FACTORY OF TERUMO CORP. from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ADMIRAL BLESENSA IMMORTAL.

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