AURORA EV-ICD™ MRI SureScan™ - Indonesia BPOM Medical Device Registration

AURORA EV-ICD™ MRI SureScan™ is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503420111. The device is manufactured by MEDTRONIC EUROPE SARL from Switzerland, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MEDTRONIC INDONESIA.

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