PureWick PW300

GUDID 00801741231001

PureWick Urine Collection System

C. R. Bard, Inc.

Bed incontinence system

• Primary Device ID: 00801741231001
• NIH Device Record Key: 2b396e24-1886-4760-9301-40404328ccb6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PureWick
• Version Model Number: PW300
• Catalog Number: PW300
• Company DUNS: 016898496
• Company Name: C. R. Bard, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: +1(844)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(844)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(844)823-5433
• Email: BMD.CS.support@bd.com

Operating and Storage Conditions

• Storage Environment Temperature: Between 41 Degrees Fahrenheit and 104 Degrees Fahrenheit
• Storage Environment Humidity: Between 25 Percent (%) Relative Humidity and 90 Percent (%) Relative Humidity
• Storage Environment Atmospheric Pressure: Between 70 KiloPascal and 106 KiloPascal
• Storage Environment Temperature: Between 41 Degrees Fahrenheit and 104 Degrees Fahrenheit
• Storage Environment Humidity: Between 25 Percent (%) Relative Humidity and 90 Percent (%) Relative Humidity
• Storage Environment Atmospheric Pressure: Between 70 KiloPascal and 106 KiloPascal

Device Identifiers

Device Issuing Agency	Device ID
GS1	00801741231001 [Primary]

FDA Product Code

• NZU: Collector, urine, powered, non indwelling catheter

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2026-02-16
• Device Publish Date: 2026-02-06

On-Brand Devices [PureWick]

• 10801741226950: PureWick Flex Female External Catheter Kit
• 10801741226462: PureWick Male External Catheter, Home Care
• 10801741226981: PureWick Flex Female External Catheter, Home Care
• 10801741226967: PureWick Flex Female External Catheter, Acute Care
• 00801741231018: PureWick Urine Collection System
• 00801741231001: PureWick Urine Collection System