RAIDER 7449

GUDID 20801902221708

Raider Guidewire 300CM

TELEFLEX INCORPORATED

Cardiac/peripheral vascular guidewire, single-use

• Primary Device ID: 20801902221708
• NIH Device Record Key: af1d77e4-6a7e-4c08-83ac-166c3da91f5f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RAIDER
• Version Model Number: IPN930524
• Catalog Number: 7449
• Company DUNS: 002348191
• Company Name: TELEFLEX INCORPORATED
• Device Count: 1
• DM Exempt: true
• 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: 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(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	10801902221701 [Primary]
GS1	20801902221708 [Package]; Contains: 10801902221701; Package: Box [5 Units]; In Commercial Distribution

FDA Product Code

• DQX: Wire, guide, catheter

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-06-12
• Device Publish Date: 2025-06-04

On-Brand Devices [RAIDER]

• 20841156108059: Raider Guidewire, 300cm
• 20841156108042: Raider Guidewire, 200cm
• 20841156111479: Raider Guidewire 200CM
• 20801902221708: Raider Guidewire 300CM