Conductor 511950-006

GUDID 00814384020451

Conductor Hydro Extra Support

CONCERT MEDICAL, LLC

Cardiac/peripheral vascular guidewire, single-use

• Primary Device ID: 00814384020451
• NIH Device Record Key: 3dcac83e-80cc-464b-a49e-4ea0a90032c4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Conductor
• Version Model Number: Extra Support
• Catalog Number: 511950-006
• Company DUNS: 189689800
• Company Name: CONCERT MEDICAL, LLC
• Device Count: 5
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00814384020444 [Unit of Use]
GS1	00814384020451 [Primary]

FDA Product Code

• DQX: Wire, Guide, 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: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-04-25

On-Brand Devices [Conductor ]

• 00814384020505: Conductor Hydro Very Floppy
• 00814384020482: Conductor Hydro Medium
• 00814384020468: Conductor Hydro Floppy
• 00814384020451: Conductor Hydro Extra Support
• 00814384020369: Extension Guidewire