ADVANCE Diagnostic Guide Wire - Indonesia BPOM Medical Device Registration

ADVANCE Diagnostic Guide Wire is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501716714. The device is manufactured by UMBRA MEDICAL PRODUCTS., INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MULTIDAYA MEDIKA.

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