CLEARVIEW®

GUDID 00885074257419

SHUNT 31150 ARTERIOTOMY 1.50MM 5PK 15LA

MEDTRONIC, INC.

Arteriovenous shunt

• Primary Device ID: 00885074257419
• NIH Device Record Key: 220f52c2-2923-434e-8fe0-3590bd5657fe
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CLEARVIEW®
• Version Model Number: 31150
• Company DUNS: 006261481
• Company Name: MEDTRONIC, INC.
• Device Count: 5
• DM Exempt: true
• 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: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Dimensions

• Outer Diameter: 1.5 Millimeter
• Outer Diameter: 1.5 Millimeter
• Outer Diameter: 1.5 Millimeter
• Outer Diameter: 1.5 Millimeter
• Outer Diameter: 1.5 Millimeter
• Outer Diameter: 1.5 Millimeter
• Outer Diameter: 1.5 Millimeter
• Outer Diameter: 1.5 Millimeter
• Outer Diameter: 1.5 Millimeter
• Outer Diameter: 1.5 Millimeter
• Outer Diameter: 1.5 Millimeter
• Outer Diameter: 1.5 Millimeter
• Outer Diameter: 1.5 Millimeter
• Outer Diameter: 1.5 Millimeter
• Outer Diameter: 1.5 Millimeter
• Outer Diameter: 1.5 Millimeter
• Outer Diameter: 1.5 Millimeter
• Outer Diameter: 1.5 Millimeter
• Outer Diameter: 1.5 Millimeter
• Outer Diameter: 1.5 Millimeter
• Outer Diameter: 1.5 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885074257419 [Unit of Use]
GS1	20885074257413 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K120612

FDA Product Code

• DWF: Catheter, cannula and tubing, vascular, cardiopulmonary bypass

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: 2020-08-04
• Device Publish Date: 2020-07-27

On-Brand Devices [CLEARVIEW®]

• 20885074257475: SHUNT, ARTERIOTOMY 31300 -3.00MM, 15LA
• 20643169423170: BLOWER/MISTER KIT 22120 CLEARVIEW 10P 15
• 00885074257464: SHUNT 31275 ARTERIOTOMY 2.75MM 5PK 15LA
• 00885074257457: SHUNT 31250 ARTERIOTOMY 2.50MM 5PK 15LA
• 00885074257440: SHUNT 31225 ARTERIOTOMY 2.25MM 5PK 15LA
• 00885074257433: SHUNT 31200 ARTERIOTOMY 2.00MM 5PK 15LA
• 00885074257426: SHUNT 31175 ARTERIOTOMY 1.75MM 5PK 15LA
• 00885074257419: SHUNT 31150 ARTERIOTOMY 1.50MM 5PK 15LA
• 00885074257402: SHUNT 31125 ARTERIOTOMY 1.25MM 5PK 15LA
• 00885074257112: SHUNT 31100 ARTERIOTOMY 1.00MM 5 PK 15LA