PROCLEIX UltrioPlex E Assay - Indonesia BPOM Medical Device Registration

PROCLEIX UltrioPlex E Assay is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30305420275. The device is manufactured by GRIFOLS DIAGNOSTIC SOLUTIONS INC from United States, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MEDQUEST JAYA GLOBAL.

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