*All of these SpeediCath® users have received compensation from Coloplast to provide this information. Each person’s situation is unique so your experience may not be the same. Talk to your healthcare provider about whether this product is right for you.

SpeediCath® sets the standard for quality catheters with innovative and compact solutions  in a range of models and sizes for men and women.

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Request your free samples by filling out the form below or call us at 1-855-814-2358.

Please note that intermittent catheters are a prescription product.  If you're requesting a sample of an intermittent catheter we require verification of a valid intermittent catheter prescription before we can send samples.   

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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.

Luja Coudé is indicated for use by patients with urine retention and patients with 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 adult male patients only. 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. 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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