PureWick PWMX30

GUDID 10801741226462

PureWick Male External Catheter, Home Care

C. R. Bard, Inc.

Urinary incontinence penis sheath/port, single-use Urinary incontinence penis sheath/port, single-use Urinary incontinence penis sheath/port, single-use Urinary incontinence penis sheath/port, single-use Urinary incontinence penis sheath/port, single-use Urinary incontinence penis sheath/port, single-use Urinary incontinence penis sheath/port, single-use Urinary incontinence penis sheath/port, single-use Urinary incontinence penis sheath/port, single-use Urinary incontinence penis sheath/port, single-use Urinary incontinence penis sheath/port, single-use Urinary incontinence penis sheath/port, single-use Urinary incontinence penis sheath/port, single-use Urinary incontinence penis sheath/port, single-use Urinary incontinence penis sheath/port, single-use Urinary incontinence penis sheath/port, single-use Urinary incontinence penis sheath/port, single-use

• Primary Device ID: 10801741226462
• NIH Device Record Key: 8c06c85d-9708-4c22-a854-027643a7048b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PureWick
• Version Model Number: PWMX30
• Catalog Number: PWMX30
• Company DUNS: 016898496
• Company Name: C. R. Bard, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• 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
• 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
• 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
• 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
• 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
• Phone: +1(844)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(844)823-5433
• Email: BMD.CS.support@bd.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00801741226465 [Primary]
GS1	10801741226462 [Package]; Contains: 00801741226465; Package: CA [30 Units]; In Commercial Distribution

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: 2024-06-10
• Device Publish Date: 2024-05-31

On-Brand Devices [PureWick]

• 10801741226950: PureWick Flex Female External Catheter Kit
• 10801741226462: PureWick Male External Catheter, Home Care