GENOSS Earloon Eustachian Tube Dilation System - Indonesia BPOM Medical Device Registration

GENOSS Earloon Eustachian Tube Dilation System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20703220123. The device is manufactured by GENOSS CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ICT WORLDWIDE INDONESIA.

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