VIMEX Fluid Pump - Indonesia BPOM Medical Device Registration

VIMEX Fluid Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603325124. The device is manufactured by VIMEX SP, Z O O. from Poland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ALLVAMED NUVACON ADIGANA.

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