DIAGAST I-Mag Diluent - Indonesia BPOM Medical Device Registration

DIAGAST I-Mag Diluent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208320896. The device is manufactured by DIAGAST from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDQUEST JAYA GLOBAL.

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