LUMIS 150 VPAP ST-A - Indonesia BPOM Medical Device Registration

LUMIS 150 VPAP ST-A is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403022749. The device is manufactured by RESMED PTY., LTD. from Australia, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. QUALTEK CONSULTANT JAKARTA.

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