AxiEM™ Spine Reference Clamp

GUDID 00763000210427

INST KIT 9735164 LIGHT REF CLAMP

MEDTRONIC NAVIGATION, INC.

Multi-purpose stereotactic surgery system Multi-purpose stereotactic surgery system Multi-purpose stereotactic surgery system Multi-purpose stereotactic surgery system Multi-purpose stereotactic surgery system Multi-purpose stereotactic surgery system Multi-purpose stereotactic surgery system Multi-purpose stereotactic surgery system Multi-purpose stereotactic surgery system Multi-purpose stereotactic surgery system Multi-purpose stereotactic surgery system Multi-purpose stereotactic surgery system Multi-purpose stereotactic surgery system Multi-purpose stereotactic surgery system

• Primary Device ID: 00763000210427
• NIH Device Record Key: 35c948be-1d16-4ec2-a244-6c494735ebe4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AxiEM™ Spine Reference Clamp
• Version Model Number: 9735164
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000210427 [Primary]

FDA Product Code

• HAW: Neurological stereotaxic Instrument

Sterilization

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

[00763000210427]

Moist Heat or Steam Sterilization

[00763000210427]

Moist Heat or Steam Sterilization

[00763000210427]

Moist Heat or Steam Sterilization

[00763000210427]

Moist Heat or Steam Sterilization

[00763000210427]

Moist Heat or Steam Sterilization

[00763000210427]

Moist Heat or Steam Sterilization

[00763000210427]

Moist Heat or Steam Sterilization

[00763000210427]

Moist Heat or Steam Sterilization

[00763000210427]

Moist Heat or Steam Sterilization

[00763000210427]

Moist Heat or Steam Sterilization

[00763000210427]

Moist Heat or Steam Sterilization

[00763000210427]

Moist Heat or Steam Sterilization

[00763000210427]

Moist Heat or Steam Sterilization

[00763000210427]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-02-17
• Device Publish Date: 2020-02-07

On-Brand Devices [AxiEM™ Spine Reference Clamp]

• 00613994233738: CLAMP 9733037 AXIEM SPINE REFERENCE
• 00643169309593: INST KIT 9735164 LIGHT REF CLAMP
• 00763000223045: CLAMP 9733037 AXIEM SPINE REFERENCE
• 00763000210427: INST KIT 9735164 LIGHT REF CLAMP