SpeediCath Flex Coudé Pro has received an overwhelmingly positive response from both users and healthcare professionals. However, we are launching this new version because we saw an opportunity to improve the opening and closure of the packaging and to reduce our environmental footprint. 

Are you interested in trying SpeediCath® Flex Coudé Pro? 

Follow the steps below:

 

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.   

 

Once you have the prescription, you can request a free sample so that you can determine whether or not the product works well for you prior to ordering.

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Important Safety Information: SpeediCath® catheters are indicated for use by patients with chronic 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. There is a separate SpeediCath Compact Set device intended for either males or females 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 catheter 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.

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