TWIN-PASS 5201

GUDID 20841156109094

Twin-Pass Torque

TELEFLEX INCORPORATED

Peripheral vascular intervention infusion catheter

• Primary Device ID: 20841156109094
• NIH Device Record Key: 5abc2fb7-1cbf-48f8-a65b-ba4ee13fad92
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TWIN-PASS
• Version Model Number: IPN922914
• Catalog Number: 5201
• 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: 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

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: 135 Centimeter
• Length: 135 Centimeter
• Length: 135 Centimeter
• Length: 135 Centimeter
• Length: 135 Centimeter
• Length: 135 Centimeter
• Length: 135 Centimeter
• Length: 135 Centimeter
• Length: 135 Centimeter
• Length: 135 Centimeter
• Length: 135 Centimeter
• Length: 135 Centimeter
• Length: 135 Centimeter
• Length: 135 Centimeter
• Length: 135 Centimeter
• Length: 135 Centimeter
• Length: 135 Centimeter
• Length: 135 Centimeter
• Length: 135 Centimeter
• Length: 135 Centimeter
• Length: 135 Centimeter
• Length: 135 Centimeter
• Length: 135 Centimeter
• Length: 135 Centimeter
• Length: 135 Centimeter
• Length: 135 Centimeter
• Length: 135 Centimeter
• Length: 135 Centimeter
• Length: 135 Centimeter
• Length: 135 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	10841156109097 [Primary]
GS1	20841156109094 [Package]; Contains: 10841156109097; Package: Box [1 Units]; In Commercial Distribution

FDA Product Code

• DQY: Catheter, percutaneous

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: 2022-08-19
• Device Publish Date: 2022-08-11

On-Brand Devices [TWIN-PASS]

• 30841156100364: Twin-Pass Torque
• 30841156100357: Twin-Pass V2, 3.5F
• 20841156107397: Twin-Pass V2
• 20841156109094: Twin-Pass Torque