Rebirth Pro2 Thrombus Aspiration Catheter - Indonesia BPOM Medical Device Registration

Rebirth Pro2 Thrombus Aspiration Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20505420090. 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 MAKO DUA MEDIKAL.

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