Bardex® Pezzer Model Drain 064022

GUDID 10801741030076

Bardex® Pezzer Model Drain Proportionate Head

C. R. Bard, Inc.

Suprapubic drainage catheter

• Primary Device ID: 10801741030076
• NIH Device Record Key: 177f2331-55f9-4373-bb42-98ca5745e5ad
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bardex® Pezzer Model Drain
• Version Model Number: 064022
• Catalog Number: 064022
• Company DUNS: 016898496
• Company Name: C. R. Bard, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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
• 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: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French
• Catheter Gauge: 22 French

Device Identifiers

Device Issuing Agency	Device ID
GS1	00801741030079 [Primary]
GS1	10801741030076 [Package]; Contains: 00801741030079; Package: CA [6 Units]; In Commercial Distribution

FDA Product Code

• FEW: Catheter, malecot

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-06-10

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