VENTURE 5823

GUDID 30841156100821

Venture 038 120cm

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: 30841156100821
• NIH Device Record Key: 63ced279-e648-4611-9f99-64cf06d036f3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VENTURE
• Version Model Number: IPN913590
• Catalog Number: 5823
• 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: 120 Centimeter
• Length: 120 Centimeter
• Length: 120 Centimeter
• Length: 120 Centimeter
• Length: 120 Centimeter
• Length: 120 Centimeter
• Length: 120 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	10841156100827 [Primary]
GS1	30841156100821 [Package]; Contains: 10841156100827; Package: Box [1 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K171335

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: 4
• Public Version Date: 2019-11-11
• Device Publish Date: 2019-01-22

On-Brand Devices [VENTURE]

• 20841156102248: Venture OTW
• 20841156102231: Venture RX
• 30841156100838: Venture 038 70cm
• 30841156100821: Venture 038 120cm
• 20841156106529: Venture .014 RX
• 20841156106512: Venture .014 OTW