GE ARIA - Indonesia BPOM Medical Device Registration

GE ARIA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501614560. The device is manufactured by YOZMA BMTECH CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GE OPERATIONS INDONESIA.

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