KEISEI Air Fluidized Support System - Indonesia BPOM Medical Device Registration

KEISEI Air Fluidized Support System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403212775. The device is manufactured by KEISEI MEDICAL INDUSTRIAL CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BLESINDO INDONESIA.

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