REVOLUTION ACT - Indonesia BPOM Medical Device Registration

REVOLUTION ACT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501711339. The device is manufactured by GE HANGWEI MEDICAL SYSTEMS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is GE OPERATIONS INDONESIA.

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