BARD® MAGNUM® Reusable Core Biopsy Instrument - Indonesia BPOM Medical Device Registration

BARD® MAGNUM® Reusable Core Biopsy Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801502851. The device is manufactured by C.R BARD. INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SCINTILLATING ASIAN CENTER.

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