Bard® Heyman™ Slipover Catheter Stylet 042900

GUDID 00801741045738

Bard® Heyman™ Slipover Catheter Stylet

C. R. Bard, Inc.

Urethral dilator, reusable Urethral dilator, reusable

• Primary Device ID: 00801741045738
• NIH Device Record Key: 16471152-e496-4060-bd2c-c84cdc3ba120
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bard® Heyman™ Slipover Catheter Stylet
• Version Model Number: 042900
• Catalog Number: 042900
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00801741045738 [Primary]

FDA Product Code

• KOE: DILATOR, URETHRAL

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-02-06
• Device Publish Date: 2016-09-21

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