VENTURE 5821

GUDID 20841156102248

Venture OTW

TELEFLEX INCORPORATED

Peripheral vascular infusion catheter

• Primary Device ID: 20841156102248
• NIH Device Record Key: 649a2297-498b-46c2-9efe-9de9f282dfce
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VENTURE
• Version Model Number: IPN914115
• Catalog Number: 5821
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	10841156102241 [Primary]
GS1	20841156102248 [Package]; Contains: 10841156102241; 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: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-04-09
• Device Publish Date: 2019-03-22

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