ENDOFLOW ® II Double Chamber - Indonesia BPOM Medical Device Registration

ENDOFLOW ® II Double Chamber is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805120133. The device is manufactured by ROCAMED FRANCE from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ADMIRAL BLESENSA IMMORTAL.

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