Medtronic Reusable Instruments & Accessories

GUDID 00763000998912

LID 5598949 LOCKING DRIVER CADDY LID

MEDTRONIC SOFAMOR DANEK, INC.

Instrument tray, reusable

• Primary Device ID: 00763000998912
• NIH Device Record Key: e9a06626-1ecb-427d-ab1a-2e209b6e8aec
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Medtronic Reusable Instruments & Accessories
• Version Model Number: 5598949
• Company DUNS: 830350380
• Company Name: MEDTRONIC SOFAMOR DANEK, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000998912 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K190840

FDA Product Code

• KCT: Sterilization wrap containers, trays, cassettes & other accessories

Sterilization

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

[00763000998912]

Moist Heat or Steam Sterilization

[00763000998912]

Moist Heat or Steam Sterilization

[00763000998912]

Moist Heat or Steam Sterilization

[00763000998912]

Moist Heat or Steam Sterilization

[00763000998912]

Moist Heat or Steam Sterilization

[00763000998912]

Moist Heat or Steam Sterilization

[00763000998912]

Moist Heat or Steam Sterilization

[00763000998912]

Moist Heat or Steam Sterilization

[00763000998912]

Moist Heat or Steam Sterilization

[00763000998912]

Moist Heat or Steam Sterilization

[00763000998912]

Moist Heat or Steam Sterilization

[00763000998912]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-09-15
• Device Publish Date: 2025-09-06

On-Brand Devices [Medtronic Reusable Instruments & Accessories]

• 00763000998912: LID 5598949 LOCKING DRIVER CADDY LID
• 00763000998905: CADDY 5598948 LOCKING DRIVER CADDY