Personal Catheter™ Intermittent Catheter 61310

GUDID 20801741068939

Personal Catheter™ Silicone Intermittent Urinary Catheter, Female

C. R. Bard, Inc.

Single-administration urethral drainage catheter Single-administration urethral drainage catheter

• Primary Device ID: 20801741068939
• NIH Device Record Key: d473feb1-6556-4c33-ab59-c8820bb78f2a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Personal Catheter™ Intermittent Catheter
• Version Model Number: 61310
• Catalog Number: 61310
• 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: 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

Device Dimensions

• Catheter Gauge: 10 French
• Catheter Gauge: 10 French

Device Identifiers

Device Issuing Agency	Device ID
GS1	00801741068935 [Primary]
GS1	10801741068932 [Package]; Contains: 00801741068935; Package: CA [30 Units]; In Commercial Distribution
GS1	20801741068939 [Package]; Contains: 10801741068932; Package: CA [180 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: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-07-23

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