DAY LISS Diluent - Indonesia BPOM Medical Device Registration

DAY LISS Diluent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208129596. The device is manufactured by HAEMOKINESIS LIMITED from Switzerland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SAKEFA.

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