MSB Reusable Instruments

GUDID 00763000916145

SCREWDRIVER EX0223017 CERVICAL

MEDTRONIC SOFAMOR DANEK, INC.

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• Primary Device ID: 00763000916145
• NIH Device Record Key: 19459838-31d7-432d-8bbc-3b16183f2200
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MSB Reusable Instruments
• Version Model Number: EX0223017
• 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: 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
• 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	00763000916145 [Primary]

FDA Product Code

• HXX: SCREWDRIVER

Sterilization

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

[00763000916145]

Moist Heat or Steam Sterilization

[00763000916145]

Moist Heat or Steam Sterilization

[00763000916145]

Moist Heat or Steam Sterilization

[00763000916145]

Moist Heat or Steam Sterilization

[00763000916145]

Moist Heat or Steam Sterilization

[00763000916145]

Moist Heat or Steam Sterilization

[00763000916145]

Moist Heat or Steam Sterilization

[00763000916145]

Moist Heat or Steam Sterilization

[00763000916145]

Moist Heat or Steam Sterilization

[00763000916145]

Moist Heat or Steam Sterilization

[00763000916145]

Moist Heat or Steam Sterilization

[00763000916145]

Moist Heat or Steam Sterilization

[00763000916145]

Moist Heat or Steam Sterilization

[00763000916145]

Moist Heat or Steam Sterilization

[00763000916145]

Moist Heat or Steam Sterilization

[00763000916145]

Moist Heat or Steam Sterilization

[00763000916145]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-04-08
• Device Publish Date: 2024-03-30

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• 00763000642303: SHAVER EX1221020 PADDLE DISTRACTOR 6MM
• 00763000648848: RETRACTOR X0821031 HAND HELD TISSUE
• 00763000876623: BOX CHISEL EX0623001 6MM W/CORONAL BEND
• 00763000583477: PROBE 5597035 MAZOR BAYONET FEELER
• 00763000638429: BLADE X07214110 CRANIAL CAUDAL R L110MM
• 00763000913885: GUARD X0423001 RIALTO DTS
• 00763000916145: SCREWDRIVER EX0223017 CERVICAL