GUDID 00613994100894

Antenna, 7440-48, Interstim, Programmer

MEDTRONIC, INC.

Multiple active implantable device programmer

• Primary Device ID: 00613994100894
• NIH Device Record Key: e21d86d9-77fe-48aa-a399-bab1008c27b3
• Commercial Distribution Discontinuation: 2018-08-13
• Commercial Distribution Status: Not in Commercial Distribution
• Version Model Number: 7440-48
• 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: false
• 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

Device Dimensions

• Length: 122 Centimeter
• Length: 122 Centimeter
• Length: 122 Centimeter
• Length: 122 Centimeter
• Length: 48 Inch
• Length: 122 Centimeter
• Length: 48 Inch
• Length: 122 Centimeter
• Length: 48 Inch
• Length: 122 Centimeter
• Length: 48 Inch
• Length: 122 Centimeter
• Length: 48 Inch
• Length: 122 Centimeter
• Length: 48 Inch
• Length: 122 Centimeter
• Length: 48 Inch
• Length: 122 Centimeter
• Length: 48 Inch
• Length: 122 Centimeter
• Length: 48 Inch
• Length: 122 Centimeter
• Length: 48 Inch
• Length: 122 Centimeter
• Length: 48 Inch
• Length: 122 Centimeter
• Length: 48 Inch
• Length: 122 Centimeter
• Length: 48 Inch
• Length: 122 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00613994100894 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P970004

FDA Product Code

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

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2018-10-22
• Device Publish Date: 2014-09-23

Devices Manufactured by MEDTRONIC, INC.

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• 00763000964603 - NA: 2024-08-12 CUSTOM PACK BB12H12R2 ADULT TABLE P
• 20763000967110 - NA: 2024-08-12 CUSTOM PACK BB12H25R 5PK 1/8 IN M/M
• 00763000967451 - NA: 2024-08-12 CUSTOM PACK BB12H59R UCHICAGOCPB3/8
• 00763000967482 - NA: 2024-08-12 CUSTOM PACK BB11M88R16 CARDIOHELP P
• 00763000946395 - DLP®: 2024-08-12 ADAPTER 10001 STRAIGHT 20PK 17L
• 00763000946517 - DLP®: 2024-08-12 CANNULA 70420 ART FLEX ARCH 20FR 20P 17L