EIZO RadiForce MX217 - Indonesia BPOM Medical Device Registration

EIZO RadiForce MX217 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501321147. The device is manufactured by EIZO CORPORATION from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TRIPUTRA TECHNO MED.

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