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 20505711746. 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 PT. MULTIDAYA MEDIKA.

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