BONHAWA Respiratory Humidifier - Indonesia BPOM Medical Device Registration

BONHAWA Respiratory Humidifier is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403420542. The device is manufactured by TELESAIR, INC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ESA MEDIKA MANDIRI.

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