LMB Manual Plasma Extractor - Indonesia BPOM Medical Device Registration

LMB Manual Plasma Extractor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20205220089. The device is manufactured by LMB TECHNOLOGIE GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is FRISMED HOSLAB INDONESIA.

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