Altaviva™

GUDID 00763000935627

KIT P7K2P001 ALTAVIVA PATIENTA^

MEDTRONIC, INC.

Implant battery charger

• Primary Device ID: 00763000935627
• NIH Device Record Key: e2b74780-3cee-4f99-b303-01107a230438
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Altaviva™
• Version Model Number: P7K2P001
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000935627 [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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-10-07
• Device Publish Date: 2025-09-29

On-Brand Devices [Altaviva™]

• 00763000936433: INS P7850N ALTAVIVA NEUROSTIMULATOR RC
• 00763000935627: KIT P7K2P001 ALTAVIVA PATIENTA^
• 00763000929367: KIT P7K2C001 ALTAVIVA CLINICIAN