AIRFIT P30i - Indonesia BPOM Medical Device Registration

AIRFIT P30i is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403420318. The device is manufactured by RESMED ASIA PTE., LTD. from Singapore, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. QUALTEK CONSULTANT JAKARTA.

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