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Contour VL™ Variable Length Percuflex® Stents


Low profile coil design, Percuflex construction and Hydro Plus™ Coating combine to set a new standard of performance for variable length ureteral stents.
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Prescriptive Information

Indications

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

Stent

Used in Procedures

Ureteroscopy

Related Medical Areas

Urology

Related Conditions

Kidney Disease Urological Conditions