GUDID 00763000140151

BLADE 9564049 1/4 TUBE S 90MM TI

MEDTRONIC SOFAMOR DANEK, INC.

Surgical retraction system, reusable

• Primary Device ID: 00763000140151
• NIH Device Record Key: 60af34c3-8715-437e-928c-d0bfa952fe3d
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 9564049
• Company DUNS: 830350380
• Company Name: MEDTRONIC SOFAMOR DANEK, 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: true
• 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

Device Dimensions

• Length: 90 Millimeter
• Length: 90 Millimeter
• Length: 90 Millimeter
• Length: 90 Millimeter
• Length: 90 Millimeter
• Length: 90 Millimeter
• Length: 90 Millimeter
• Length: 90 Millimeter
• Length: 90 Millimeter
• Length: 90 Millimeter
• Length: 90 Millimeter
• Length: 90 Millimeter
• Length: 90 Millimeter
• Length: 90 Millimeter
• Length: 90 Millimeter
• Length: 90 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000140151 [Primary]

FDA Product Code

• GAD: RETRACTOR

Sterilization

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

[00763000140151]

Moist Heat or Steam Sterilization

[00763000140151]

Moist Heat or Steam Sterilization

[00763000140151]

Moist Heat or Steam Sterilization

[00763000140151]

Moist Heat or Steam Sterilization

[00763000140151]

Moist Heat or Steam Sterilization

[00763000140151]

Moist Heat or Steam Sterilization

[00763000140151]

Moist Heat or Steam Sterilization

[00763000140151]

Moist Heat or Steam Sterilization

[00763000140151]

Moist Heat or Steam Sterilization

[00763000140151]

Moist Heat or Steam Sterilization

[00763000140151]

Moist Heat or Steam Sterilization

[00763000140151]

Moist Heat or Steam Sterilization

[00763000140151]

Moist Heat or Steam Sterilization

[00763000140151]

Moist Heat or Steam Sterilization

[00763000140151]

Moist Heat or Steam Sterilization

[00763000140151]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-10-04
• Device Publish Date: 2021-09-24

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• 00763000856830 - VERTE-STACK® Spinal System: 2025-08-26 IMPLANT 6240164 ANATOMIC 16X14X11MM
• 00763000856854 - VERTE-STACK® Spinal System: 2025-08-26 IMPLANT 6240641 ANATOMIC 14X11X6MM