Bard® Interglide™ Intermittent Catheter 430612

GUDID 10801741077941

Interglide™ Female Coated Intermittent Catheter

C. R. Bard, Inc.

Single-administration urethral drainage catheter

• Primary Device ID: 10801741077941
• NIH Device Record Key: 106cb76e-6b13-436b-b018-65a6ced41dd0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bard® Interglide™ Intermittent Catheter
• Version Model Number: 430612
• Catalog Number: 430612
• 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: 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

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00801741077944 [Primary]
GS1	10801741077941 [Package]; Contains: 00801741077944; Package: CA [25 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K951260

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

On-Brand Devices [Bard® Interglide™ Intermittent Catheter]

• 10801741078054: Interglide™ Standard Coated Intermittent Catheter
• 10801741078047: Interglide™ Standard Coated Intermittent Catheter
• 10801741078030: Interglide™ Standard Coated Intermittent Catheter
• 10801741078023: Interglide™ Standard Coated Intermittent Catheter
• 10801741078016: Interglide™ Standard Coated Intermittent Catheter
• 10801741078009: Interglide™ Standard Coated Intermittent Catheter
• 10801741077996: Interglide™ Pediatric Coated Intermittent Catheter
• 10801741077989: Interglide™ Pediatric Coated Intermittent Catheter
• 10801741077972: Interglide™ Female Coated Intermittent Catheter
• 10801741077965: Interglide™ Female Coated Intermittent Catheter
• 10801741077958: Interglide™ Female Coated Intermittent Catheter
• 10801741077941: Interglide™ Female Coated Intermittent Catheter
• 10801741077934: Interglide™ Female Coated Intermittent Catheter
• 10801741077927: Interglide™ Female Coated Intermittent Catheter