Medtronic Reusable Instruments

GUDID 00763000606183

BLADE EX0921060 DOUBLE THK AND WD 17CM

MEDTRONIC MINIMED, INC.

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• 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

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• 00763000827151 - inpen™: 2024-06-10 KIT MMT-105ELBLNA INPEN ELI LILLY BLUE