Medtronic Reusable Instruments

GUDID 00763000606183

BLADE EX0921060 DOUBLE THK AND WD 17CM

MEDTRONIC MINIMED, INC.

Surgical retraction system, reusable

• Primary Device ID: 00763000606183
• NIH Device Record Key: 7d6ca385-5124-41a2-bed8-a1cdbeeb6b0b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Medtronic Reusable Instruments
• Version Model Number: EX0921060
• Company DUNS: 849626338
• Company Name: MEDTRONIC MINIMED, 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	00763000606183 [Primary]

FDA Product Code

• GAD: RETRACTOR

Sterilization

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

[00763000606183]

Moist Heat or Steam Sterilization

[00763000606183]

Moist Heat or Steam Sterilization

[00763000606183]

Moist Heat or Steam Sterilization

[00763000606183]

Moist Heat or Steam Sterilization

[00763000606183]

Moist Heat or Steam Sterilization

[00763000606183]

Moist Heat or Steam Sterilization

[00763000606183]

Moist Heat or Steam Sterilization

[00763000606183]

Moist Heat or Steam Sterilization

[00763000606183]

Moist Heat or Steam Sterilization

[00763000606183]

Moist Heat or Steam Sterilization

[00763000606183]

Moist Heat or Steam Sterilization

[00763000606183]

Moist Heat or Steam Sterilization

[00763000606183]

Moist Heat or Steam Sterilization

[00763000606183]

Moist Heat or Steam Sterilization

[00763000606183]

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 MINIMED, INC.

• 00199150034123 - SFTWR MMT-6101 AHCL APP 3.1 ANDROID: 2025-10-06 SFTWR MMT-6101 AHCL APP 3.1 ANDROID
• 00199150034130 - MiniMed Mobile App: 2025-10-06 SFTWR MMT-6102 AHCL APP 3.1 IOS
• 00763000721350 - Simplera™: 2025-07-16 SFTWR MMT-8400 1.1 CGM MODULE IOS US
• 00763000721367 - Simplera™: 2025-07-16 SFTWR MMT-8401 1.1 CGM MODULE ANDROID US
• 00199150003686 - MiniMed™ 780G: 2025-06-27 PUMP MMT-1884G 780G 6.21 GS
• 00763000960018 - MiniMed™ 780G: 2025-06-27 Kit MMT-1894 780G US A2.01 6.42U
• 00763000960025 - MiniMed™ 780G: 2025-06-27 KIT MMT-1894MD 780G US GOV 6.42U A2.01 S
• 00763000960049 - MiniMed™ 780G: 2025-06-27 PUMP MMT-1884 780G US MG A2.01 6.41U PRB