WARRIOR 7388

GUDID 30841156101156

Warrior Guidewire 200cm

TELEFLEX INCORPORATED

Cardiac/peripheral vascular guidewire, single-use

• Primary Device ID: 30841156101156
• NIH Device Record Key: d1d171a4-bade-421e-a005-748ebfd5f978
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: WARRIOR
• Version Model Number: IPN914142
• Catalog Number: 7388
• Company DUNS: 002348191
• Company Name: TELEFLEX INCORPORATED
• 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: true
• 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(919)544-8000
• Email: CS@TELEFLEX.COM

Device Dimensions

• Length: 200 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	10841156101152 [Primary]
GS1	30841156101156 [Package]; Contains: 10841156101152; Package: Box [5 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K180128

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: 2019-11-11
• Device Publish Date: 2019-06-11

On-Brand Devices [WARRIOR]

• 30841156101156: Warrior Guidewire 200cm
• 30841156101163: Warrior Guidewire 300cm
• 20841156108035: Warrior Guidewire, 200cm
• 20801902168003: Warrior Guidewire, 300cm