ADVIA 120/ ADVIA 2120/ ADVIA 2120i OPTIpoint - Indonesia BPOM Medical Device Registration

ADVIA 120/ ADVIA 2120/ ADVIA 2120i OPTIpoint is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208127271. The device is manufactured by FISHER DIAGNOSTICS, from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SIEMENS HEALTHINEERS INDONESIA.

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