BEGRAFT Coronary Stent Graft System - Indonesia BPOM Medical Device Registration

BEGRAFT Coronary Stent Graft System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503817723. The device is manufactured by BENTLEY INNOMED GMBH from Germany, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. NUGRA KARSERA.

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