Percutaneous Nephrostomy Dilators

Percutaneous nephrostomy dilators from Coloplast prepare a tract during PCNL procedures.  The dilators are constricted of firm, kink-resistant material and include a tapered distal tip for atraumatic placement.

Firm and Atraumatic Construction

  • Kink-resistant material
  • Tapered distal tip for atraumatic placement and maneuverability

Simple Dilators and Sets

  • Single sized dilators available in 8F, 10F, and 12F
  • RBB010 dilator set includes: 6F, 8F, and 10F simple dilators
  • RBB014 dilator set includes: 6F, 8F, 10F, 12F, and 14F simple dilators
  • RBC008 dilator set includes: 6F, 8F simple dilators and a splittable working sheath
  • RBC010 dilator set includes: 6F, 8F, 11F simple dilators and a splittable working sheath
Item Description Sales UOM EA / Sales UOM
RBA008 8F Simple Dilator Retail Box 5
RBA010 10F Simple Dilator Retail Box 5
RBA012 12F Simple Dilator Retail Box 5
RBB010 6F, 8F, 10F Dilator Set Set 1
RBB014 6F, 8F, 10F, 12F, 14F Dilator Set Set 1
RBC008 6F, 8F Dilator Set with Splittable Working Sheath Set 1
RBC010 6F, 8F, 11F Dilator Set with Splittable Working Sheath Set 1

Indications

Dilator for tract preparation or splittable working sheath to protect the parenchyma.

Contraindications

Any contraindication to PCN surgical procedure among which urinary tract infection or coagulation disorders that should be treated before the procedure unless the situation is an absolute emergency.  The evaluation of the allergic background of a patient is the health care professional’s responsibility.  Do not use, when, in the judgement of the physician, such a procedure would be contrary to the best interest of the patient.

Warnings and Precautions

This type of device should only be used by trained and experienced professionals.

Any use other than stated indications is under the responsibility of the physician.

Reuse of this single use product may create a potential risk to the user. Reprocessing, cleaning, disinfection and sterilization may compromise product characteristics which in turn create an additional risk of physical harm to or infection of the patient.

Adverse Events

As with any dilation or percutaneous access creation, the use of the PCN dilators may cause but are not limited to: bleeding, hematuria, tissue trauma, urinary infection.

There is a risk of damage to the kidney, urinary tract or neighboring organs, particularly if the instructions for use have not been complied with, and especially if the procedure has been performed without ultrasound or fluoroscopic control.

Potential Complications

Complications from the use of this device should be brought to the immediate attention of your Coloplast Representative and your physician.

The information provided is not comprehensive with regard to product risks.  For a comprehensive listing of indications, contraindications, warnings, and precautions refer to the product’s Instructions for Use.  Alternatively, you may contact a Coloplast representative at 1-800-258-3476 and/or visit the company Website at www.coloplast.com.

For Rx Only

Caution: Federal (USA) law restricts this device to sale by or on the order of a physician.

Minneapolis, MN

04/08/2020

Request Additional Information

I understand that by providing all of the below information and clicking “Send”, I am giving Coloplast my consent to be contacted for the reasons I described in my message.