TIMESH System

GUDID 00721902583094

CASE 176-851 MASTER IMPLANT TRAY CADDY

MEDTRONIC SOFAMOR DANEK, INC.

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• Primary Device ID: 00721902583094
• NIH Device Record Key: f24e6338-2c32-4823-9bf0-6021d06dd6e1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TIMESH System
• Version Model Number: 176-851
• 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
• 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
• 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	00721902583094 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K190840

FDA Product Code

• FSM: TRAY, SURGICAL, INSTRUMENT

Sterilization

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

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

[00721902583094]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-03-08
• Device Publish Date: 2021-02-28

On-Brand Devices [TIMESH System]

• 00721902583131: CASE 176-855 IMPLANT TRAY FD
• 00721902583124: CASE 176-854 IMPLANT TRAY GP
• 00721902583100: CASE 176-852 MASTER IMPLANT TRAY LID
• 00721902583094: CASE 176-851 MASTER IMPLANT TRAY CADDY
• 00721902582011: CASE 853-700 OUTER CASE