Bard® Eagle® Inflation Device 325130

GUDID 00801741067259

Bard® Eagle® Inflation Device

C. R. Bard, Inc.

Catheter/overtube balloon inflator, single-use

• Primary Device ID: 00801741067259
• NIH Device Record Key: abc440ae-0595-427d-afe1-99f822af6851
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bard® Eagle® Inflation Device
• Version Model Number: 325130
• Catalog Number: 325130
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00801741067259 [Primary]

FDA Product Code

• KOE: DILATOR, URETHRAL

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-05-06
• Device Publish Date: 2017-10-12

On-Brand Devices [Bard® Eagle® Inflation Device]

• 00801741067259: Bard® Eagle® Inflation Device
• 00801741067242: Bard® Eagle® Inflation Device