Nephrostomy catheters
Percuflex Urinary Diversion Stent
by Boston Scientific Corporation
A sterile non-bioabsorbable tubular device intended to be implanted in an obstructed ureter (e.g., from stone, stricture, compression, fibrosis, trauma) to maintain luminal patency allowing urine to drain from the renal pelvis to the bladder. It is made of a synthetic polymer(s) [e.g., polytetrafluoroethylene (PTFE), polyethylene (PE), silicone], sometimes with a hydrophilic coating (e.g., hydrogel), and may have various designs (e.g., continuous tube with or without drainage side holes, covered or non-covered mesh structure). Disposable devices intended to assist implantation may be included. The device is typically intended for long-term, but not permanent, implantation.
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Where to buy Percuflex Urinary Diversion Stent
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Percuflex Urinary Diversion Stent models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| M0061603250 | — | Not stated | Available |
| M0061603300 | — | Not stated | Available |
| M0061603350 | — | Not stated | Available |
| M0061604250 | — | Not stated | Available |
| M0061604300 | — | Not stated | Available |
| M0061604350 | — | Not stated | Available |
| M0061605250 | — | Not stated | Available |
| M0061605300 | — | Not stated | Available |
| M0061605350 | — | Not stated | Available |
Procedures that use nephrostomy catheters
Frequently asked questions
What is Percuflex Urinary Diversion Stent used for?
A sterile non-bioabsorbable tubular device intended to be implanted in an obstructed ureter (e.g., from stone, stricture, compression, fibrosis, trauma) to maintain luminal patency allowing urine to drain from the renal pelvis to the bladder. It is made of a synthetic polymer(s) [e.g., polytetrafluoroethylene (PTFE), polyethylene (PE), silicone], sometimes with a hydrophilic coating (e.g., hydrogel), and may have various designs (e.g., continuous tube with or without drainage side holes, covered or non-covered mesh structure). Disposable devices intended to assist implantation may be included. The device is typically intended for long-term, but not permanent, implantation.
Who makes Percuflex Urinary Diversion Stent?
Percuflex Urinary Diversion Stent is made by Boston Scientific Corporation. It is listed under nephrostomy and nephroureteral catheters in our device library.
What sizes does Percuflex Urinary Diversion Stent come in?
The FDA device database does not list sizes for Percuflex Urinary Diversion Stent. Check the instructions for use or ask a Boston Scientific Corporation representative.
Is Percuflex Urinary Diversion Stent MRI safe?
The FDA device database entry for Percuflex Urinary Diversion Stent does not state its MRI safety status. Check the labeling before MRI.
Is Percuflex Urinary Diversion Stent FDA cleared?
Percuflex Urinary Diversion Stent is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Boston Scientific Corporation sales representative?
Boston Scientific Corporation has not listed representatives on LA Vascular yet. Visit the Boston Scientific Corporation company page for contact details.
Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.