LIOFERON Tb/LTBI Human Blood Simulation Tubes - Indonesia BPOM Medical Device Registration

LIOFERON Tb/LTBI Human Blood Simulation Tubes is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303420007. The device is manufactured by LIONEX GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FAITHFUL MEDICAL GRACE.

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