SATORI Arterial - Venous Fistula Set - Indonesia BPOM Medical Device Registration

SATORI Arterial - Venous Fistula Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805320973. The device is manufactured by HOSPITECH MANUFACTURING SERVICE SDN. BHD. from Malaysia, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is GOLDEN GLOBE MEDICA.

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