Bard® Ureteral Catheter Adapter 140000

GUDID 20801741130476

Bard® Ureteral Catheter Adapter

C. R. Bard, Inc.

Urethral/suprapubic catheter valve-connector

• Primary Device ID: 20801741130476
• NIH Device Record Key: 6f6b2fc5-fe3a-4600-a125-de4f92380402
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bard® Ureteral Catheter Adapter
• Version Model Number: 140000
• Catalog Number: 140000
• Company DUNS: 016898496
• Company Name: C. R. Bard, Inc.
• Device Count: 24
• 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: true
• OTC Over-The-Counter: false

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
• 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	00801741130472 [Unit of Use]
GS1	10801741130479 [Primary]
GS1	20801741130476 [Package]; Contains: 10801741130479; Package: CA [24 Units]; In Commercial Distribution

FDA Product Code

• KOD: CATHETER, UROLOGICAL

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2023-07-31
• Device Publish Date: 2017-12-11

Devices Manufactured by C. R. Bard, Inc.

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• 10801741226981 - PureWick: 2024-08-06 PureWick Flex Female External Catheter, Home Care
• 10801741226462 - PureWick: 2024-06-10 PureWick Male External Catheter, Home Care
• 10801741226950 - PureWick: 2024-06-10 PureWick Flex Female External Catheter Kit
• 10801741218788 - SureStep Foley Tray System: 2024-05-21 SureStep Foley Tray Kit optimized for Sensica UO System
• 10801741218832 - SureStep Foley Tray System: 2024-05-21 SureStep Foley Tray Kit optimized for Sensica UO System
• 10801741171663 - Bardia: 2023-08-29 Bardia Silicone Elastomer Coated Foley Catheter
• 20801741171677 - Bardia: 2023-08-29 Bardia Silicone Elastomer Coated Foley Catheter