FLEXIMAG MAX 500 Adult Neonatal Pediatric Electronic Lung Ventilator - Indonesia BPOM Medical Device Registration

FLEXIMAG MAX 500 Adult Neonatal Pediatric Electronic Lung Ventilator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403124758. The device is manufactured by MAGNAMED MEDICAL TECHNOLOGY S/A from Brazil, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is BETA MEDICAL.

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