AEROGEN PRO - Indonesia BPOM Medical Device Registration

AEROGEN PRO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403818539. The device is manufactured by AEROGEN LTD. from Ireland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ANDRA PRIMA JAYA.

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