ACOMA'S HI-500 - Indonesia BPOM Medical Device Registration

ACOMA'S HI-500 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501220273. The device is manufactured by GEMSS CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. POSCOM ACOMA INDONESIA.

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