LUMIFY Diagnostic Ultrasound System iOS - Indonesia BPOM Medical Device Registration

LUMIFY Diagnostic Ultrasound System iOS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501026368. The device is manufactured by PHILIPS ULTRASOUND INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PHILIPS INDONESIA COMMERCIAL.

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