Percutaneous Nephrostomy Dilators

Firm and Atraumatic Construction

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

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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.

Reuse of this single use product may create a potential risk to the user.

Potential Complications
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.

The information provided is not comprehensive with regard to product risks. For a comprehensive listing of indications, contraindications, warnings, precautions, and adverse events 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.

Caution: Federal law (USA) restricts this device to sale by or on the order of a physician.
Minneapolis, MN
12/07/2021
PM-19617