RESMED APNEALINK AIR - Indonesia BPOM Medical Device Registration

RESMED APNEALINK AIR is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20402914151. The device is manufactured by RESMED PTY., LTD. from Australia, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. QUALTEK CONSULTANT JAKARTA.

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