NIDEK Refraction System - Indonesia BPOM Medical Device Registration

NIDEK Refraction System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201814308. The device is manufactured by NIDEK CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is MULYA HUSADA JAYA.

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