ALLPLEX™ GI-Bacteria(II) Assay - Indonesia BPOM Medical Device Registration

ALLPLEX™ GI-Bacteria(II) Assay is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303420655. The device is manufactured by SEEGENE INC. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SCIENCEWERKE.

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