If your current prescription is for a category A4351 catheter (straight tip), contact your doctor to see if a category A4352 catheter (coudé tip) like SpeediCath® Flex Coudé Pro might be right for you. If you and your doctor determine that SpeediCath® Flex Coudé Pro is right for you, ask your doctor to write a prescription for it. Documentation of difficulty using a straight tip catheter will be required in order to change your prescription.

Important Safety Information: SpeediCath® Flex Coudé Pro and SpeediCath Flex Coudé Pro Pocket are indicated is indicated for use by patients with urine retention and patients with a post void residual volume (PVR) due to neurogenic and non-neurogenic voiding dysfunction. The catheter is inserted into the urethra to reach the bladder allowing urine to drain. The product is for male patients only. SpeediCath catheters are available by prescription only. Patients performing self-catheterization should follow the advice of, and direct questions about use of the product to, their medical professional. Before using the device, carefully read the product labels and information accompanying the device including the instructions for use which contain additional safety information. The SpeediCath product is for single-use only; discard it after use. If you experience symptoms of a urinary tract infection, or are unable to pass the catheter into the bladder, contact your healthcare professional. The risk information provided here is not comprehensive. To learn more, talk to your healthcare provider. For further information, call Coloplast Corp. at 1-866-226-6362 and/or consult the company website at www.coloplast.us.

Reimbursement disclaimer: Coloplast Corp. provides this information for your general reference and related to the reimbursement of Coloplast products only. Reimbursement, coverage and payment policies can vary from one insurer and region to another, and may change over time. Coloplast does not guarantee coverage or payment of products.