HOSPITECH Guedel Airway - Indonesia BPOM Medical Device Registration

HOSPITECH Guedel Airway is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403700851. The device is manufactured by HOSPITECH MANUFACTURING SERVICES SDH., BHD. from Malaysia, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. SCINTILLATING ASIAN CENTER.

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