Tunneled dialysis catheters
Catheter Repair Kit
A collection of devices intended to repair an in situ central venous catheter by replacing the damaged external (proximal) portion of the catheter. It includes the replacement proximal section of the catheter and devices associated with the adhesion of this section to the catheter portion remaining in situ (e.g., adhesive material, needle, syringe, sleeve); a complete central venous catheter is not included. This is a single-use device.
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Where to buy Catheter Repair Kit
Contact Bard Access Systems, Inc. directly; they can quote, ship, or point you to the distributor for your country.
From bd.com, checked October 2026.
No reply, or outside their markets? Send us a request and we route it to a rep or distributor for your country.
Catheter Repair Kit 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 |
|---|---|---|---|
| 5581000 | — | MR Conditional | Available |
Procedures that use tunneled dialysis catheters
Frequently asked questions
What is Catheter Repair Kit used for?
A collection of devices intended to repair an in situ central venous catheter by replacing the damaged external (proximal) portion of the catheter. It includes the replacement proximal section of the catheter and devices associated with the adhesion of this section to the catheter portion remaining in situ (e.g., adhesive material, needle, syringe, sleeve); a complete central venous catheter is not included. This is a single-use device.
Who makes Catheter Repair Kit?
Catheter Repair Kit is made by Bard Access Systems, Inc.. It is listed under tunneled dialysis catheters (permcath) in our device library.
What sizes does Catheter Repair Kit come in?
The FDA device database does not list sizes for Catheter Repair Kit. Check the instructions for use or ask a Bard Access Systems, Inc. representative.
Is Catheter Repair Kit MRI safe?
The FDA device database lists Catheter Repair Kit as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Catheter Repair Kit FDA cleared?
Catheter Repair Kit is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Bard Access Systems, Inc. sales representative?
Bard Access Systems, Inc. has not listed representatives on LA Vascular yet. Visit the Bard Access Systems, Inc. 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.