PureWick Female External Catheter PWFX30

GUDID 20801741189054

PureWick Female External Catheter, Not Made with Natural Rubber Latex

C. R. Bard, Inc.

Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use Female wearable urinal, single-use

• Primary Device ID: 20801741189054
• NIH Device Record Key: ea35649e-cf2e-46c8-b950-30a91a7549c9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PureWick Female External Catheter
• Version Model Number: PWFX30
• Catalog Number: PWFX30
• 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(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com
• Phone: +1(800)526-4455
• Email: medical.services@crbard.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00801741189050 [Primary]
GS1	10801741189057 [Package]; Contains: 00801741189050; Package: CA [1 Units]; In Commercial Distribution
GS1	20801741189054 [Package]; Contains: 10801741189057; 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: 2020-08-14
• Device Publish Date: 2020-08-06

On-Brand Devices [PureWick Female External Catheter]

• 20801741189054: PureWick Female External Catheter, Not Made with Natural Rubber Latex
• 20801741183618: PureWick Female External Catheter, Not Made with Natural Rubber Latex, Kit
• 10801741163088: PureWick Female External Catheter, Not Made with Natural Rubber Latex
• 20801741143087: PureWick Female External Catheter
• 20801741215937: PureWick Female External Catheter