Medtronic

GUDID 00763000942809

REF SET 9735500 SPINE REFRENCING

MEDTRONIC NAVIGATION, INC.

Multi-purpose stereotactic surgery system

• Primary Device ID: 00763000942809
• NIH Device Record Key: f04a2f2d-3569-4010-be2a-88c39037dc96
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Medtronic
• Version Model Number: 9735500
• Company DUNS: 835233107
• Company Name: MEDTRONIC NAVIGATION, 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000942809 [Primary]

FDA Product Code

• OLO: Orthopedic stereotaxic instrument

Sterilization

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

[00763000942809]

Moist Heat or Steam Sterilization

[00763000942809]

Moist Heat or Steam Sterilization

[00763000942809]

Moist Heat or Steam Sterilization

[00763000942809]

Moist Heat or Steam Sterilization

[00763000942809]

Moist Heat or Steam Sterilization

[00763000942809]

Moist Heat or Steam Sterilization

[00763000942809]

Moist Heat or Steam Sterilization

[00763000942809]

Moist Heat or Steam Sterilization

[00763000942809]

Moist Heat or Steam Sterilization

[00763000942809]

Moist Heat or Steam Sterilization

[00763000942809]

Moist Heat or Steam Sterilization

[00763000942809]

Moist Heat or Steam Sterilization

[00763000942809]

Moist Heat or Steam Sterilization

[00763000942809]

Moist Heat or Steam Sterilization

[00763000942809]

Moist Heat or Steam Sterilization

[00763000942809]

Moist Heat or Steam Sterilization

[00763000942809]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-11-19
• Device Publish Date: 2024-11-11

On-Brand Devices [Medtronic]

• 00763000922405: INST SET 9733935 CRANIAL PASSIVE
• 00763000927141: REF SET 9735501 SPINE REF REVISION
• 00763000942809: REF SET 9735500 SPINE REFRENCING