GUDID 00763000763152

SW APP P7A2C11 ALTAVIVA CLINICIAN

MEDTRONIC, INC.

Implantable electrical stimulation device management software

• Primary Device ID: 00763000763152
• NIH Device Record Key: 410725c7-ee20-4749-9aab-39e59ff7f5a7
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: P7A2C11
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000763152 [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

Devices Manufactured by MEDTRONIC, INC.

• 00763000764234 - NA: 2026-04-01 CUSTOM PACK CB11Z66R 1/4 LOOP
• 00763000764241 - NA: 2026-04-01 CUSTOM PACK CB11Z68R CDI PACK
• 00763000764319 - NA: 2026-04-01 CUSTOM PACK HY2G71R9 ST. AGNES PK
• 00763000764951 - NA: 2026-04-01 CUSTOM PACK BB12A73R AV LOOP
• 00763000770419 - NA: 2026-04-01 CUSTOM PACK 11Z79R1 VALVE SK LN
• 00763000770433 - NA: 2026-04-01 CUSTOM PACK BB12B18R HIIT FUS
• 00763000774127 - NA: 2026-04-01 CUSTOM PACK BB11U49R3 ADULT QUANTUM
• 00763000791421 - NA: 2026-04-01 CUSTOM PACK BB11Y57R5 HEART LUNG