Iris Diluent Pack - Indonesia BPOM Medical Device Registration

Iris Diluent Pack is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208120485. The device is manufactured by BECKMAN COULTER INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is DHH TRADING INDONESIA.

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