GUDID 00763000140267

HOLDER 9564006 ENDOSCOPE 16

MEDTRONIC SOFAMOR DANEK, INC.

Surgical retraction system, reusable

• Primary Device ID: 00763000140267
• NIH Device Record Key: fdc11a0e-79eb-4e98-acba-64ea53553862
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 9564006
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00763000140267 [Primary]

FDA Product Code

• GAD: RETRACTOR

Sterilization

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

[00763000140267]

Moist Heat or Steam Sterilization

[00763000140267]

Moist Heat or Steam Sterilization

[00763000140267]

Moist Heat or Steam Sterilization

[00763000140267]

Moist Heat or Steam Sterilization

[00763000140267]

Moist Heat or Steam Sterilization

[00763000140267]

Moist Heat or Steam Sterilization

[00763000140267]

Moist Heat or Steam Sterilization

[00763000140267]

Moist Heat or Steam Sterilization

[00763000140267]

Moist Heat or Steam Sterilization

[00763000140267]

Moist Heat or Steam Sterilization

[00763000140267]

Moist Heat or Steam Sterilization

[00763000140267]

Moist Heat or Steam Sterilization

[00763000140267]

Moist Heat or Steam Sterilization

[00763000140267]

Moist Heat or Steam Sterilization

[00763000140267]

Moist Heat or Steam Sterilization

[00763000140267]

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.

• 00199150002108 - Medtronic Reusable Instruments: 2025-06-09 SCREWDRIVER X2150100 MT25
• 00199150002115 - Medtronic Reusable Instruments: 2025-06-09 RETENTIVE X2151160 SLEEVE
• 00763000829933 - N/a: 2025-06-09 TRAY 5597907 SAS SV CEMENT DELIV DRIVER
• 00763000883461 - N/a: 2025-06-09 LOCK SLEEVE 7480756T LOCK SLEEVE
• 00763000883478 - N/a: 2025-06-09 SHAFT 7480757T MAS CEMENT DELIVERY
• 00763000883485 - N/a: 2025-06-09 SHAFT 7480758T SAS CEMENT DELIVERY
• 00763000884529 - N/A: 2025-06-09 TAP 7080920 4.0 X 13MM TAP
• 00763000889012 - ATLANTIS® Anterior Cervical Plate System: 2025-06-09 SCREW 3125413 4.5 X 13 SELF DRILL FIX