GUDID 00763000929374

WIRELESS RECHARGER P720R1 ALTAVIVA

MEDTRONIC, INC.

Implant battery charger

• Primary Device ID: 00763000929374
• NIH Device Record Key: 8ad13ed3-b967-42d5-a017-2e7d415d42de
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: P720R1
• Company DUNS: 006261481
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000929374 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P240011

FDA Product Code

• QPT: Stimulator, tibial, electrical, implantable, for urinary incontinence

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2025-12-15
• Device Publish Date: 2025-10-02

Devices Manufactured by MEDTRONIC, INC.

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• 00763000659233 - SimuForm™: 2026-02-09 RING 7800RR30 SIMUFORM SR 30MM MDR
• 00763000659240 - SimuForm™: 2026-02-09 RING 7800RR32 SIMUFORM SR 32MM MDR
• 00763000659257 - SimuForm™: 2026-02-09 RING 7800RR34 SIMUFORM SR 34MM MDR
• 00763000659264 - SimuForm™: 2026-02-09 RING 7800RR36 SIMUFORM SR 36MM MDR