PureWick PWF030FX

GUDID 10801741226967

PureWick Flex Female External Catheter, Acute Care

C. R. Bard, Inc.

Female wearable urinal, single-use

• Primary Device ID: 10801741226967
• NIH Device Record Key: b97f307c-6a32-4c8e-ba29-40f17ac766bf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PureWick
• Version Model Number: PWF030FX
• Catalog Number: PWF030FX
• Company DUNS: 016898496
• Company Name: C. R. Bard, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Conditional
• 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(800)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(800)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(800)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(800)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(800)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(800)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(800)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(800)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(800)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(800)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(800)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(800)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(800)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(800)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(800)823-5433
• Email: BMD.CS.support@bd.com
• Phone: +1(800)823-5433
• Email: BMD.CS.support@bd.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00801741226960 [Primary]
GS1	10801741226967 [Package]; Contains: 00801741226960; Package: CA [30 Units]; In Commercial Distribution
GS1	20801741226964 [Package]; Package: BX [6 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: 2024-08-06
• Device Publish Date: 2024-07-29

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