GBO DUODYNATOR - Indonesia BPOM Medical Device Registration

GBO DUODYNATOR is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403614658. The device is manufactured by GBO MEDIZINTECHNIK AG. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. IT'S YOUR INDONESIA.

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