R350 7390

GUDID 50841156101174

R350 V2 Guidewire

TELEFLEX INCORPORATED

Cardiac/peripheral vascular guidewire, single-use

• Primary Device ID: 50841156101174
• NIH Device Record Key: 0682bfe8-17ce-4d82-a2e6-16d6544943dc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: R350
• Version Model Number: IPN913606
• Catalog Number: 7390
• 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
• 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
• 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
• 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
• 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 Dimensions

• Length: 350 Centimeter
• Length: 350 Centimeter
• Length: 350 Centimeter
• Length: 350 Centimeter
• Length: 350 Centimeter
• Length: 350 Centimeter
• Length: 350 Centimeter
• Length: 350 Centimeter
• Length: 350 Centimeter
• Length: 350 Centimeter
• Length: 350 Centimeter
• Length: 350 Centimeter
• Length: 350 Centimeter
• Length: 350 Centimeter
• Length: 350 Centimeter
• Length: 350 Centimeter
• Length: 350 Centimeter
• Length: 350 Centimeter
• Length: 350 Centimeter
• Length: 350 Centimeter
• Length: 350 Centimeter
• Length: 350 Centimeter
• Length: 350 Centimeter
• Length: 350 Centimeter
• Length: 350 Centimeter
• Length: 350 Centimeter
• Length: 350 Centimeter
• Length: 350 Centimeter
• Length: 350 Centimeter
• Length: 350 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	50841156101174 [Package]; Contains: 60841156101171; Package: Box [5 Units]; Discontinued: 2022-11-17; In Commercial Distribution
GS1	60841156101171 [Primary]

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: 2021-06-25
• Device Publish Date: 2021-06-17

On-Brand Devices [R350]

• 50841156101174: R350 V2 Guidewire
• 20841156111448: R350 Guidewire