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WebModel Number FF803R: Device Problem Break (1069) Patient Problem No Known Impact Or Consequence To Patient (2692) Event Type malfunction Manufacturer Narrative Investigation: the investigation was performed using a … WebThe Global Unique Device Identification Database (GUDID) contains key device identification information submitted to the FDA about medical devices that have Unique Device Identifiers (UDI). WebModel Number FF803R: Device Problem Break (1069) Patient Problem Device Embedded In Tissue or Plaque (3165) Event Type malfunction Manufacturer Narrative オーバーロード 強いキャラ