Accessories, Catheter, G-U
FDA product code KNY · Class 2 · 20 devices · 56 reports · 16 devices named in recalls
- UroPass 61238BXGyrus ACMI, LLC · ACCESSORIES, CATHETER, G-U1 recall10 reports
- UroPass 61024BXGyrus ACMI, LLC · ACCESSORIES, CATHETER, G-U1 recall5 reports
- UroPass 61138BXGyrus ACMI, LLC · ACCESSORIES, CATHETER, G-U1 recall5 reports
- UroPass 61046BXGyrus ACMI, LLC · ACCESSORIES, CATHETER, G-U1 recall4 reports
- UroPass 61054BXGyrus ACMI, LLC · ACCESSORIES, CATHETER, G-U1 recall4 reports
- UroPass 61146BXGyrus ACMI, LLC · ACCESSORIES, CATHETER, G-U1 recall4 reports
- UroPass 61224BXGyrus ACMI, LLC · ACCESSORIES, CATHETER, G-U1 recall4 reports
- UroPass 61254BXGyrus ACMI, LLC · ACCESSORIES, CATHETER, G-U1 recall4 reports
- UroPass 61324BXGyrus ACMI, LLC · ACCESSORIES, CATHETER, G-U1 recall3 reports
- UroPass 61338BXGyrus ACMI, LLC · ACCESSORIES, CATHETER, G-U1 recall2 reports
- UroPass 61154BXGyrus ACMI, LLC · ACCESSORIES, CATHETER, G-U1 recall1 report
- UroPass 61246BXGyrus ACMI, LLC · ACCESSORIES, CATHETER, G-U1 recall1 report
- UroPass 61346BXGyrus ACMI, LLC · ACCESSORIES, CATHETER, G-U1 recall1 report
- GYRUS ACMI, INC 61038BXGyrus ACMI, LLC · ACCESSORIES, CATHETER, G-U1 recall0 reports
- UroPass 61124BXGyrus ACMI, LLC · ACCESSORIES, CATHETER, G-U1 recall0 reports
- UroPass 61354BXGyrus ACMI, LLC · ACCESSORIES, CATHETER, G-U1 recall0 reports
- UroWire® Guidewire with SL-6® Hydrophilic Coating B8634Applied Medical Resources Corporation · Accessories, Catheter, G-U5 reports
- Acucise® Endopyelotomy System B1005Applied Medical Resources Corporation · Accessories, Catheter, G-U1 report
- Bard® Large Nylon Catheter Plug 0414LC. R. Bard, Inc. · ACCESSORIES, CATHETER, G-U1 report
- ACUCISE® PROCEDURAL PACK UNIVERSAL PACK A BK002Applied Medical Resources Corporation · Accessories, Catheter, G-U1 report