GUDID 00763000970062

SW APP A51200 GU CLINICIAN MICRO EU MDR

MEDTRONIC, INC.

Multiple active implantable device programmer

• Primary Device ID: 00763000970062
• NIH Device Record Key: a5a033d5-25c4-494a-9028-3a01c3d852f4
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: A51200
• 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
• 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	00763000970062 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P080025

FDA Product Code

• QON: Implanted electrical device intended for treatment of fecal 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: 2025-06-27
• Device Publish Date: 2025-06-19

Devices Manufactured by MEDTRONIC, INC.

• 20763000558332 - HR HTC: 2026-03-03 CARTRIDGE 402-07 HR HTC BXD 20BX
• 00199150003709 - Sphere-9™ Catheter: 2026-03-02 CATHETER AFR-00001 SPHERE 9 US GAL
• 20763000558189 - CLOTtrac™: 2026-03-02 CONTROL 550-01 CLOTTRAC CWB
• 20763000558196 - CLOTtrac™: 2026-03-02 CONTROL 550-07 CLOTTRAC HR 15BX
• 20763000558202 - CLOTtrac™: 2026-03-02 CONT 550-08 CLOTTRAC HR ABN BXD ASY
• 20763000558219 - CLOTtrac™: 2026-03-02 CONT 550-09 CLOTTRAC LR ABN BXD ASY
• 20763000558226 - CLOTtrac™: 2026-03-02 CONT 550-10 CLOTTRAC RACT ABN
• 20763000558233 - CLOTtrac™: 2026-03-02 CONTROL 550-12 CLOTTRAC HTC