CA-MI NEW ASKIR 230/12V BR Suction Unit - Indonesia BPOM Medical Device Registration

CA-MI NEW ASKIR 230/12V BR Suction Unit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603212972. The device is manufactured by CA-MI S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is FA ANTARES MEDIKA.

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