None

GUDID 00613994203632

CASE 7220010L OUTER LID

MEDTRONIC SOFAMOR DANEK, INC.

Instrument tray

• Primary Device ID: 00613994203632
• NIH Device Record Key: eca700cf-d081-4e28-ba19-aa670fa26af8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: None
• Version Model Number: 7220010L
• 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: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00613994203632 [Primary]

FDA Product Code

• FSM: TRAY, SURGICAL, INSTRUMENT

Sterilization

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

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

[00613994203632]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-08-09
• Device Publish Date: 2017-10-30

On-Brand Devices [None]

• 00613994325006: CAS 9790941 PREFIXATION PIN CADDY
• 00613994318855: LID 6240007 LID ANATOMIC
• 00613994248404: CASE 2940099 INSERTER REMOVAL TRAY
• 00613994203762: CASE 6279003 CRNRSTN PSR DLX ST 576 U TR
• 00613994203717: CASE 7229325L IMPLANT TRAY LID
• 00613994203632: CASE 7220010L OUTER LID
• 00613994143174: CASE 9059102 MESH CUTTER TRAY