SFRI Diluton H18 - Indonesia BPOM Medical Device Registration

SFRI Diluton H18 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208129904. The device is manufactured by SFRI SARL. from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MITRA BAHAGIA CITRA MEDIKA.

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