AMBU Aura-I Single Use Laryngeal Mask - Indonesia BPOM Medical Device Registration

AMBU Aura-I Single Use Laryngeal Mask is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403420018. The device is manufactured by AMBU., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. AMI MEDIKA INDONESIA.

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