BIOREMA Polyethersulfone Low Flux Series - Indonesia BPOM Medical Device Registration

BIOREMA Polyethersulfone Low Flux Series is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805124561. The device is manufactured by ALLMED MEDICAL GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TRADING COMPANY MENDJANGAN.

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