GUDID 00643169314399

PROBE 8225751 BALL TIP W/STIM 2.3MM ROHS

MEDTRONIC XOMED, INC.

Nerve-locating system, line-powered

• Primary Device ID: 00643169314399
• NIH Device Record Key: e7d65853-e4a3-4d0e-ba0a-f78ba59c761f
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 8225751
• Company DUNS: 835465063
• Company Name: MEDTRONIC XOMED, 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: true
• 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

Device Dimensions

• Outer Diameter: 2.3 Millimeter
• Outer Diameter: 2.3 Millimeter
• Outer Diameter: 2.3 Millimeter
• Outer Diameter: 2.3 Millimeter
• Outer Diameter: 2.3 Millimeter
• Outer Diameter: 2.3 Millimeter
• Outer Diameter: 2.3 Millimeter
• Outer Diameter: 2.3 Millimeter
• Outer Diameter: 2.3 Millimeter
• Outer Diameter: 2.3 Millimeter
• Outer Diameter: 2.3 Millimeter
• Outer Diameter: 2.3 Millimeter
• Outer Diameter: 2.3 Millimeter
• Outer Diameter: 2.3 Millimeter
• Outer Diameter: 2.3 Millimeter
• Outer Diameter: 2.3 Millimeter
• Outer Diameter: 2.3 Millimeter
• Outer Diameter: 2.3 Millimeter
• Outer Diameter: 2.3 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00643169314399 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K031510

FDA Product Code

• GWF: STIMULATOR, ELECTRICAL, EVOKED RESPONSE

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-04-07

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• 00763000548797 - Hydrodebrider: 2026-02-23 HYDRODEBRIDER 1914001 STD HANDPIECE ROHS
• 00763000548803 - Hydrodebrider: 2026-02-23 HANDPIECE 1921002 HYDRODEBRID FRNTL ROHS
• 20763000888910 - Merocel: 2026-02-23 PACKING 400151 100PK MICRO SPHERES 4MM
• 20763000888927 - Merocel: 2026-02-23 PACKING 400152 100PK MICRO SPHERES 5MM