FUJI Medical Dry Imaging Film DI-HT - Indonesia BPOM Medical Device Registration

FUJI Medical Dry Imaging Film DI-HT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11501613735. The device is manufactured by FUJIFILM MATERIAL MANUFACTURING CO., LTD from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is FUJIFILM INDONESIA.

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