SureTrak

GUDID 00763000209643

INST KIT 9735162 SURETRAK II CLAMP DRVR

MEDTRONIC NAVIGATION, INC.

Multi-purpose stereotactic surgery system

• Primary Device ID: 00763000209643
• NIH Device Record Key: a4dabd7e-6167-4490-a2e7-c34011d7f613
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SureTrak
• Version Model Number: 9735162
• 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: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000209643 [Primary]

FDA Product Code

• HAW: Neurological stereotaxic Instrument

Sterilization

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

[00763000209643]

Moist Heat or Steam Sterilization

[00763000209643]

Moist Heat or Steam Sterilization

[00763000209643]

Moist Heat or Steam Sterilization

[00763000209643]

Moist Heat or Steam Sterilization

[00763000209643]

Moist Heat or Steam Sterilization

[00763000209643]

Moist Heat or Steam Sterilization

[00763000209643]

Moist Heat or Steam Sterilization

[00763000209643]

Moist Heat or Steam Sterilization

[00763000209643]

Moist Heat or Steam Sterilization

[00763000209643]

Moist Heat or Steam Sterilization

[00763000209643]

Moist Heat or Steam Sterilization

[00763000209643]

Moist Heat or Steam Sterilization

[00763000209643]

Moist Heat or Steam Sterilization

[00763000209643]

Moist Heat or Steam Sterilization

[00763000209643]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-01-14
• Device Publish Date: 2018-12-13

On-Brand Devices [SureTrak]

• 00643169279865: INST KIT 9735162 SURETRAK II CLAMP DRVR
• 00643169279858: INST KIT 9735161 SURETRAK II TRCKR TRAY
• 00763000209643: INST KIT 9735162 SURETRAK II CLAMP DRVR
• 00763000927226: SURETRAK2 961-574 PASSIVE SYSTEM