PHOENIX One DS - Indonesia BPOM Medical Device Registration

PHOENIX One DS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805611750. The device is manufactured by NIPRO PURE WATER GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MAIN WHEEL BEAM.

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