GUDID 00763000140076

BLADE 9564038 1/4 TUBE 80MM TI

MEDTRONIC SOFAMOR DANEK, INC.

Surgical retraction system, reusable

• Primary Device ID: 00763000140076
• NIH Device Record Key: 4ea1bd87-c71f-470e-98c6-f1522693e215
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 9564038
• 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: 80 Millimeter
• Length: 80 Millimeter
• Length: 80 Millimeter
• Length: 80 Millimeter
• Length: 80 Millimeter
• Length: 80 Millimeter
• Length: 80 Millimeter
• Length: 80 Millimeter
• Length: 80 Millimeter
• Length: 80 Millimeter
• Length: 80 Millimeter
• Length: 80 Millimeter
• Length: 80 Millimeter
• Length: 80 Millimeter
• Length: 80 Millimeter
• Length: 80 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000140076 [Primary]

FDA Product Code

• GAD: RETRACTOR

Sterilization

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

[00763000140076]

Moist Heat or Steam Sterilization

[00763000140076]

Moist Heat or Steam Sterilization

[00763000140076]

Moist Heat or Steam Sterilization

[00763000140076]

Moist Heat or Steam Sterilization

[00763000140076]

Moist Heat or Steam Sterilization

[00763000140076]

Moist Heat or Steam Sterilization

[00763000140076]

Moist Heat or Steam Sterilization

[00763000140076]

Moist Heat or Steam Sterilization

[00763000140076]

Moist Heat or Steam Sterilization

[00763000140076]

Moist Heat or Steam Sterilization

[00763000140076]

Moist Heat or Steam Sterilization

[00763000140076]

Moist Heat or Steam Sterilization

[00763000140076]

Moist Heat or Steam Sterilization

[00763000140076]

Moist Heat or Steam Sterilization

[00763000140076]

Moist Heat or Steam Sterilization

[00763000140076]

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

Devices Manufactured by MEDTRONIC SOFAMOR DANEK, INC.

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• 00763000703639 - Medtronic Reusable Instruments: 2025-07-21 CAM SPREADER TRIAL 4010014 12 DEG 14MM