GETINGE Rotaflow II System - Indonesia BPOM Medical Device Registration

GETINGE Rotaflow II System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504420096. The device is manufactured by MAQUET CARDIOPULMONARY GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is INDOSOPHA SAKTI.

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