DUMOLABS S. Paratyphi AH - Indonesia BPOM Medical Device Registration

DUMOLABS S. Paratyphi AH is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303121389. The device is manufactured by DIALAB G.M.B.H. from Austria, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DUMO DIAGNOSTICS INDONESIA.

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