GUDID 00763000517182

SW APP A51300 OASIS CLINICIAN GU

MEDTRONIC, INC.

Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer

• Primary Device ID: 00763000517182
• NIH Device Record Key: 8461d938-070f-48f1-8ab6-f1c926f79554
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: A51300
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000517182 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P080025

FDA Product Code

• EZW: Stimulator, electrical, implantable, for 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: 2022-03-14
• Device Publish Date: 2022-03-04

Devices Manufactured by MEDTRONIC, INC.

• 20763000770291 - TrailBlazer™: 2024-07-16 PS ASC-014-090 TRAILBLAZER ANGLED V04
• 20763000770307 - TrailBlazer™: 2024-07-16 PS ASC-014-135 TRAILBLAZER ANGLED V04
• 20763000770314 - TrailBlazer™: 2024-07-16 PS ASC-014-150 TRAILBLAZER ANGLED V04
• 20763000770321 - TrailBlazer™: 2024-07-16 PS ASC-018-090 TRAILBLAZER ANGLED V04
• 20763000770338 - TrailBlazer™: 2024-07-16 PS ASC-018-135 TRAILBLAZER ANGLED V04
• 20763000770345 - TrailBlazer™: 2024-07-16 PS ASC-018-150 TRAILBLAZER ANGLED V04
• 20763000770352 - TrailBlazer™: 2024-07-16 PS ASC-035-065 TRAILBLAZER ANGLED V04
• 20763000770369 - TrailBlazer™: 2024-07-16 PS ASC-035-090 TRAILBLAZER ANGLED V04