PureWick Male External Catheter, Home Care
PureWick - PWMX30
Device Description
A device intended to be worn on or over the penis by an incontinent patient to channel urine from the penis, via a tube, into a collection bag. It consists of a penis-worn sheath (e.g., condom-catheter) or adhesive port (e.g., glans penis attachment), and may include a portion of tubing; the bag is not included. This device provides an alternative to inserting a catheter through the urethra, especially when difficulty is encountered in insertion or retention. It may be used to treat urinary incontinence or for non-ambulatory patients. This is a single-use device.
Environmental Conditions
No Data Available
Device Sizes
No Data Available
Device Sterilization
Device Sterile: False
Sterilization Prior To Use: False
Sterilization Methods: No Data Available
Product Codes
Code: NZU
Device Name: Collector, Urine, Powered, Non Indwelling Catheter
Device Class: 1
Physical State: The device consists of a female designed cup, male cup, collection tubing, urine bag, pump, rechargeable batter, circuitry to control the operaton of the pump, software, and carrying case to be attached to a wheel chair or beside.
Definition: For the non-invasive, non-sterile collection of urine and for patients unable to void on their own or have control of voiding. Often patient confined to the bed or a wheelchair.
Submission Type ID: 4
Review Panel: GU
Review Code: N/A
Technical Method: Y
Gmp Exempt Flag: Urine is collected in a collection cup and with the assistance of a battery powered pump the urine is drawn through tubing into a urine bag for storage.
Life Sustain Support Flag: N
Unclassified Reason: N/A
Implant Flag: N
Target Area: The collection cup is place under the external meatus of the urethra
Regulation Number: 876.5250
Third Party Flag: N
Medical Specialty: GU
Device IdentifiersDevice Id: 10801741226462
Device Type: Package
DeviceId Issuing Agency: GS1
Contains DI Number: 00801741226465
Package Quantity: 30
Package Discontinue Date: N/A
Package Status: In Commercial Distribution
Package Type: CA
Device Id: 00801741226465
Device Type: Primary
DeviceId Issuing Agency: GS1
Contains DI Number: N/A
Package Quantity: N/A
Package Discontinue Date: N/A
Package Status: N/A
Package Type: N/A