GUDID 00613994803665

KIT 9003 A INTL ONLY SHUNT CONT SM LO

MEDTRONIC PS MEDICAL, INC.

Ventriculo-peritoneal/atrial shunt

• Primary Device ID: 00613994803665
• NIH Device Record Key: ddc6a1c0-0169-4706-831a-f8ed9c043a24
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 9003 A
• Company DUNS: 089055867
• Company Name: MEDTRONIC PS MEDICAL, INC.
• 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: false
• 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(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

• Length: 90 Centimeter
• Length: 90 Centimeter
• Length: 90 Centimeter
• Length: 90 Centimeter
• Length: 90 Centimeter
• Length: 90 Centimeter
• Outer Diameter: 2.5 Millimeter
• Device Size Text, specify: 0
• Length: 90 Centimeter
• Outer Diameter: 2.5 Millimeter
• Device Size Text, specify: 0
• Length: 90 Centimeter
• Outer Diameter: 2.5 Millimeter
• Device Size Text, specify: 0
• Length: 90 Centimeter
• Outer Diameter: 2.5 Millimeter
• Device Size Text, specify: 0
• Length: 90 Centimeter
• Outer Diameter: 2.5 Millimeter
• Device Size Text, specify: 0
• Length: 90 Centimeter
• Outer Diameter: 2.5 Millimeter
• Device Size Text, specify: 0
• Length: 90 Centimeter
• Outer Diameter: 2.5 Millimeter
• Device Size Text, specify: 0
• Length: 90 Centimeter
• Outer Diameter: 2.5 Millimeter
• Device Size Text, specify: 0
• Length: 90 Centimeter
• Outer Diameter: 2.5 Millimeter
• Device Size Text, specify: 0
• Length: 90 Centimeter
• Outer Diameter: 2.5 Millimeter
• Device Size Text, specify: 0
• Length: 90 Centimeter
• Outer Diameter: 2.5 Millimeter
• Device Size Text, specify: 0
• Length: 90 Centimeter
• Outer Diameter: 2.5 Millimeter
• Device Size Text, specify: 0
• Length: 90 Centimeter
• Outer Diameter: 2.5 Millimeter
• Device Size Text, specify: 0
• Length: 90 Centimeter
• Outer Diameter: 2.5 Millimeter
• Device Size Text, specify: 0
• Length: 90 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00613994803665 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K841442

FDA Product Code

• JXG: Shunt, central nervous system and components

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: 2018-07-06
• Device Publish Date: 2015-06-23

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