Medtronic Reusable Instruments

GUDID 00763000606169

BLADE EX0921058 DOUBLE THK AND WD 15CM

MEDTRONIC NAVIGATION, INC.

Surgical retraction system, reusable

• Primary Device ID: 00763000606169
• NIH Device Record Key: 903a8df6-f206-4794-9fce-c674dae2ca7b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Medtronic Reusable Instruments
• Version Model Number: EX0921058
• Company DUNS: 835233107
• Company Name: MEDTRONIC NAVIGATION, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000606169 [Primary]

FDA Product Code

• GAD: RETRACTOR

Sterilization

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

[00763000606169]

Moist Heat or Steam Sterilization

[00763000606169]

Moist Heat or Steam Sterilization

[00763000606169]

Moist Heat or Steam Sterilization

[00763000606169]

Moist Heat or Steam Sterilization

[00763000606169]

Moist Heat or Steam Sterilization

[00763000606169]

Moist Heat or Steam Sterilization

[00763000606169]

Moist Heat or Steam Sterilization

[00763000606169]

Moist Heat or Steam Sterilization

[00763000606169]

Moist Heat or Steam Sterilization

[00763000606169]

Moist Heat or Steam Sterilization

[00763000606169]

Moist Heat or Steam Sterilization

[00763000606169]

Moist Heat or Steam Sterilization

[00763000606169]

Moist Heat or Steam Sterilization

[00763000606169]

Moist Heat or Steam Sterilization

[00763000606169]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-10-18
• Device Publish Date: 2022-10-10

Devices Manufactured by MEDTRONIC NAVIGATION, INC.

• 00763000927127 - Medtronic: 2024-12-13 INST SET 9735283 SOLERA 5.5/6.0 DRVR
• 00763000927189 - Medtronic: 2024-12-13 INST SET 9734495 REFERENCING STD
• 00763000927233 - Medtronic: 2024-12-13 INST SET 9734494 TACTILE PROBES
• 00763000922412 - Medtronic: 2024-11-25 INST SET 9733935 CRANIAL PASSIVE
• 00763000927035 - NavLock™: 2024-11-25 INST SET 9734833 UNIVERSAL NAVLOCK
• 00763000927042 - NavLock™: 2024-11-25 INST SET 9734834 CAPSTONE TRIALS
• 00763000927059 - NavLock™: 2024-11-25 INST SET 9734835 CLYDESDALE TRIALS
• 00763000927066 - Medtronic: 2024-11-25 INST SET 9734836 TLIF/DLIF INSERTER