Woven Phillips Follower Urethral Bougie 024012

GUDID 00801741073298

Woven Phillips Follower Urethral Bougie

C. R. Bard, Inc.

Urethral dilator, reusable

• Primary Device ID: 00801741073298
• NIH Device Record Key: 1d65381f-72cb-4c25-b537-311f95f83dc7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Woven Phillips Follower Urethral Bougie
• Version Model Number: 024012
• Catalog Number: 024012
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• 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
• 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 Dimensions

• Catheter Gauge: 12 French
• Catheter Gauge: 12 French
• Catheter Gauge: 12 French
• Catheter Gauge: 12 French
• Catheter Gauge: 12 French
• Catheter Gauge: 12 French
• Catheter Gauge: 12 French
• Catheter Gauge: 12 French
• Catheter Gauge: 12 French
• Catheter Gauge: 12 French
• Catheter Gauge: 12 French
• Catheter Gauge: 12 French
• Catheter Gauge: 12 French
• Catheter Gauge: 12 French

Device Identifiers

Device Issuing Agency	Device ID
GS1	00801741073298 [Primary]

FDA Product Code

• FBW: FILIFORM AND FILIFORM FOLLOWER

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-09-14
• Device Publish Date: 2020-09-04

On-Brand Devices [Woven Phillips Follower Urethral Bougie]

• 00801741073359: Woven Phillips Follower Urethral Bougie
• 00801741073342: Woven Phillips Follower Urethral Bougie
• 00801741073335: Woven Phillips Follower Urethral Bougie
• 00801741073328: Woven Phillips Follower Urethral Bougie
• 00801741073311: Woven Phillips Follower Urethral Bougie
• 00801741073304: Woven Phillips Follower Urethral Bougie
• 00801741073298: Woven Phillips Follower Urethral Bougie
• 00801741073281: Woven Phillips Follower Urethral Bougie
• 00801741073274: Woven Phillips Follower Urethral Bougie