Indicated for extrinsic compression of ureter, ureteral obstruction, ureteral trauma, ureteral manipulation, preparation for ureteral manipulation and assistance with stone fragment passage.
Contraindications
Contraindicated for poor surgical risk patients, unexplained hematuria and un-repaired ureteral avulsion.
Warnings
For single use only. Do not reuse, reprocess or resterilize.
Potential Adverse Effects
The Potential Complications, which may result from a ureteral stent procedure, include ureteral reflux, extravasation, cathter occlusion, catheter dislodgment, hemorrhage, sepsis, perforation of the urinary tract, and peritonitis. Products with HydroPlus Coating may cause slight irritation in some individuals.
Cautions
NOTE: Where long-term use is indicated, it is recommended that indwelling time not exceed 365 days. This stent should be evaluated by the physician on or before 90 days postplacement.
Federal (USA) law and governing law outside the USA restricts these devices to sale by or on the order of a physician.
Trademark
Percuflex, Contour, Hydro Plus, and Nautilus are trademarks of Boston Scientific Corporation or its affiliates.
Product Type
StentUsed in Procedures
UreteroscopyRelated Medical Areas
UrologyRelated Conditions
Kidney Disease Urological Conditions