KINE-SIM - Indonesia BPOM Medical Device Registration

KINE-SIM is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403220209. The device is manufactured by KINESIQ INC. from Canada, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. AIRINDO MEDIKA CENTER.

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