MIZUHO Head Frame - Indonesia BPOM Medical Device Registration

MIZUHO Head Frame is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21002220072. The device is manufactured by MIZUHO CORPORATION, GOSEN FACTORY from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SIGMA KARSA MAGNA.

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