SUPERCROSS 5340

GUDID 30841156100470

SuperCross 014 FT 130cm

TELEFLEX INCORPORATED

Peripheral vascular infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter

• Primary Device ID: 30841156100470
• NIH Device Record Key: ef495aaa-7eea-4eb5-9c47-4f796b6bcbb5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SUPERCROSS
• Version Model Number: IPN913555
• Catalog Number: 5340
• 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

Device Dimensions

• Length: 130 Centimeter
• Length: 130 Centimeter
• Length: 130 Centimeter
• Length: 130 Centimeter
• Length: 130 Centimeter
• Length: 130 Centimeter
• Length: 130 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	10841156100476 [Primary]
GS1	30841156100470 [Package]; Contains: 10841156100476; Package: Box [1 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K101659

FDA Product Code

• DQY: Catheter, percutaneous

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-04-09
• Device Publish Date: 2018-11-08

On-Brand Devices [SUPERCROSS]

• 30841156100494: SuperCross 014 FT 150cm
• 30841156100470: SuperCross 014 FT 130cm
• 30841156100463: SuperCross AT 90 Degree XT 150cm
• 30841156100456: SuperCross AT 90 Degree XT 130cm
• 30841156100449: SuperCross AT 120 Degree 150cm
• 30841156100432: SuperCross AT 120 Degree 130cm
• 30841156100425: SuperCross AT 90 Degree 150cm
• 30841156100418: SuperCross AT 90 Degree 130cm
• 30841156100401: SuperCross AT 45 Degree 150cm
• 30841156100395: SuperCross AT 45 Degree 130cm
• 30841156100388: SuperCross 150cm 014
• 30841156100371: SuperCross 130cm 014
• 20841156107472: SuperCross 014 AT, 90 Degree XT, 150cm
• 20841156107465: SuperCross 014 AT, 90 Degree XT, 130cm
• 20841156107458: SuperCross 014 AT, 120 Degree, 150cm
• 20841156107441: SuperCross 014 AT, 120 Degree, 130cm
• 20841156107434: SuperCross 014 AT, 90 Degree, 150cm
• 20841156107427: SuperCross 014 AT, 90 Degree, 130cm
• 20841156107410: SuperCross 014 AT, 45 Degree, 150cm
• 20841156107403: SuperCross 014 AT, 45 Degree, 130cm