GUDID 00721902593642

EXTENSION 748910 QUAD IN LINE,LOW Z,10CM

MEDTRONIC, INC.

Neural-tissue electrical stimulation lead Neural-tissue electrical stimulation lead Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension

• Primary Device ID: 00721902593642
• NIH Device Record Key: 1b5b2093-c07b-49ac-8595-8e9c5c5e9b17
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 748910
• Company DUNS: 796986144
• Company Name: MEDTRONIC, 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: false
• Serial Number: true
• 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
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Dimensions

• Length: 10 Centimeter
• Length: 10 Centimeter
• Length: 10 Centimeter
• Length: 10 Centimeter
• Length: 10 Centimeter
• Length: 10 Centimeter
• Length: 10 Centimeter
• Length: 10 Centimeter
• Length: 10 Centimeter
• Length: 10 Centimeter
• Length: 10 Centimeter
• Length: 10 Centimeter
• Length: 10 Centimeter
• Length: 10 Centimeter
• Length: 10 Centimeter
• Length: 10 Centimeter
• Length: 10 Centimeter
• Length: 10 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00721902593642 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P840001

FDA Product Code

• LGW: STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF

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: 2014-09-23

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