AGFA Hardcopy Imager System Drystar - Indonesia BPOM Medical Device Registration

AGFA Hardcopy Imager System Drystar is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501811860. The device is manufactured by AGFA-GEVAERT HEALTHCARE GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is GEVAERT AGFA HEALTHCARE INDONESIA.

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