PureWick Male PWM030

GUDID 10801741219150

PureWick Male External Catheter Kit

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

• Primary Device ID: 10801741219150
• NIH Device Record Key: b861bef3-46f3-4944-9b55-7d9999ebff8f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PureWick Male
• Version Model Number: PWM030
• Catalog Number: PWM030
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00801741219153 [Primary]
GS1	10801741219150 [Package]; Contains: 00801741219153; 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: 2022-08-09
• Device Publish Date: 2022-08-01

Devices Manufactured by C. R. Bard, Inc.

• 10801741171663 - Bardia: 2023-08-29 Bardia Silicone Elastomer Coated Foley Catheter
• 20801741171677 - Bardia: 2023-08-29 Bardia Silicone Elastomer Coated Foley Catheter
• 20801741171684 - Bardia: 2023-08-29 Bardia Silicone Elastomer Coated Foley Catheter
• 20801741171691 - Bardia: 2023-08-29 Bardia Silicone Elastomer Coated Foley Catheter
• 20801741171707 - Bardia: 2023-08-29 Bardia Silicone Elastomer Coated Foley Catheter
• 10801741171717 - Bardia: 2023-08-29 Bardia Silicone Elastomer Coated Foley Catheter
• 10801741171724 - Bardia: 2023-08-29 Bardia Silicone Elastomer Coated Foley Catheter
• 10801741171731 - Bardia: 2023-08-29 Bardia Silicone Elastomer Coated Foley Catheter