Medtronic Reusable Instruments

GUDID 00763000606176

BLADE EX0921059 DOUBLE THK AND WD 16CM

MEDTRONIC XOMED, INC.

Surgical retraction system, reusable

• Primary Device ID: 00763000606176
• NIH Device Record Key: 5d0673b8-3fad-463d-bfe8-06afa22de95f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Medtronic Reusable Instruments
• Version Model Number: EX0921059
• Company DUNS: 835465063
• Company Name: MEDTRONIC XOMED, 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	00763000606176 [Primary]

FDA Product Code

• GAD: RETRACTOR

Sterilization

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

[00763000606176]

Moist Heat or Steam Sterilization

[00763000606176]

Moist Heat or Steam Sterilization

[00763000606176]

Moist Heat or Steam Sterilization

[00763000606176]

Moist Heat or Steam Sterilization

[00763000606176]

Moist Heat or Steam Sterilization

[00763000606176]

Moist Heat or Steam Sterilization

[00763000606176]

Moist Heat or Steam Sterilization

[00763000606176]

Moist Heat or Steam Sterilization

[00763000606176]

Moist Heat or Steam Sterilization

[00763000606176]

Moist Heat or Steam Sterilization

[00763000606176]

Moist Heat or Steam Sterilization

[00763000606176]

Moist Heat or Steam Sterilization

[00763000606176]

Moist Heat or Steam Sterilization

[00763000606176]

Moist Heat or Steam Sterilization

[00763000606176]

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 XOMED, INC.

• 00643169547087 - NIM®: 2025-09-22 MAINFRAME 8253402 NEURO 3.0 INTL EL ROHS
• 00763000745080 - NuVent™: 2025-08-25 INFLATOR KIT 18INFKIT BALLOON
• 00763000831479 - NIM™: 2025-08-19 PROBE NIMDTP35 ENDO 35CM 1MM BALL TIP
• 20763000831480 - NIM™: 2025-08-19 PROBE 8225490X 3PK INCREMENTING 1MM TIP
• 20763000831497 - NIM™: 2025-08-19 PROBE 8225825X 3PK INCREMT STD PRASS TIP
• 00763000309480 - Causse/Polycel: 2025-07-01 PROSTHESIS 1156376 CAUSSE FLPL PARTIAL
• 20763000870359 - Microgel: 2025-07-01 VENT TUBE 1082201 5PK PAPA TYPE 1.14
• 20763000870366 - Sheehy: 2025-07-01 VENT TUBE 1083301 5PK SHEEHY TYPE 1.27