Guide Glide Guidewire Introducer Needle 0720658

GUDID 20801741086872

Intro Needle, 21ga x 7cm

Bard Access Systems, Inc.

Vascular catheter introduction needle Vascular catheter introduction needle

• Primary Device ID: 20801741086872
• NIH Device Record Key: 2c88012b-23a8-43a7-b124-c17f95742396
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Guide Glide Guidewire Introducer Needle
• Version Model Number: 0720658
• Catalog Number: 0720658
• Company DUNS: 044611812
• Company Name: Bard Access Systems, 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)545-0890
• Email: medical.services@crbard.com
• Phone: +1(800)545-0890
• Email: medical.services@crbard.com

Device Dimensions

• Length: 70 Millimeter
• Length: 70 Millimeter
• Length: 70 Millimeter
• Length: 70 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00801741086878 [Primary]
GS1	10801741086875 [Package]; Contains: 00801741086878; Package: BX [25 Units]; In Commercial Distribution
GS1	20801741086872 [Package]; Contains: 10801741086875; Package: CA [8 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K082580

FDA Product Code

• DYB: INTRODUCER, CATHETER

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-16

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