Bard® Nelaton Catheters 8014300

GUDID 10801741124096

Bard® Nelaton Catheters

C. R. Bard, Inc.

Single-administration urethral drainage catheter

• Primary Device ID: 10801741124096
• NIH Device Record Key: 5eda1821-6c77-49a6-aba8-3cb35ebcd9a9
• Commercial Distribution Discontinuation: 2021-02-02
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Bard® Nelaton Catheters
• Version Model Number: 8014300
• Catalog Number: 8014300
• Company DUNS: 016898496
• Company Name: C. R. Bard, Inc.
• Device Count: 12
• 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: true
• Labeled No Natural Rubber Latex: false
• 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

Device Dimensions

• Catheter Gauge: 30 French
• Length: 16 Inch
• Catheter Gauge: 30 French
• Length: 16 Inch
• Catheter Gauge: 30 French
• Length: 16 Inch
• Catheter Gauge: 30 French
• Length: 16 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00801741124099 [Unit of Use]
GS1	10801741124096 [Primary]

FDA Product Code

• KOD: CATHETER, UROLOGICAL

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2025-12-19
• Device Publish Date: 2016-07-23

On-Brand Devices [Bard® Nelaton Catheters]

• 10801741124096: Bard® Nelaton Catheters
• 10801741122627: Bard® Nelaton Catheters
• 10801741122610: Bard® Nelaton Catheters
• 10801741122603: Bard® Nelaton Catheters
• 10801741122597: Bard® Nelaton Catheters
• 10801741122580: Bard® Nelaton Catheters
• 10801741122573: Bard® Nelaton Catheters
• 10801741122559: Bard® Nelaton Catheters
• 10801741122542: Bard® Nelaton Catheters
• 10801741122535: Bard® Nelaton Catheters
• 10801741122528: Bard® Nelaton Catheters
• 10801741122511: Bard® Nelaton Catheters