RUSCH – PE Guedel Airway - Indonesia BPOM Medical Device Registration

RUSCH – PE Guedel Airway is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403914037. The device is manufactured by FOREMOUNT ENTERPRISE CO., LTD. from Taiwan (China), and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. LABORA MANDIRI INDO PRATAMA.

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