CROSSTRAC 72203158

GUDID 00885554022223

MTO ASSEMBLY BULLET CROSSTRAC II

Smith & Nephew, Inc.

Orthopaedic implant calibration pin

• Primary Device ID: 00885554022223
• NIH Device Record Key: c71cfba9-640c-4129-8c43-686a75bfd063
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CROSSTRAC
• Version Model Number: 72203158
• Catalog Number: 72203158
• Company DUNS: 109903521
• Company Name: Smith & Nephew, 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)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885554022223 [Primary]

FDA Product Code

• NBH: ACCESSORIES,ARTHROSCOPIC

Sterilization

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

[00885554022223]

Moist Heat or Steam Sterilization

[00885554022223]

Moist Heat or Steam Sterilization

[00885554022223]

Moist Heat or Steam Sterilization

[00885554022223]

Moist Heat or Steam Sterilization

[00885554022223]

Moist Heat or Steam Sterilization

[00885554022223]

Moist Heat or Steam Sterilization

[00885554022223]

Moist Heat or Steam Sterilization

[00885554022223]

Moist Heat or Steam Sterilization

[00885554022223]

Moist Heat or Steam Sterilization

[00885554022223]

Moist Heat or Steam Sterilization

[00885554022223]

Moist Heat or Steam Sterilization

[00885554022223]

Moist Heat or Steam Sterilization

[00885554022223]

Moist Heat or Steam Sterilization

[00885554022223]

Moist Heat or Steam Sterilization

[00885554022223]

Moist Heat or Steam Sterilization

[00885554022223]

Moist Heat or Steam Sterilization

[00885554022223]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-01-31
• Device Publish Date: 2015-08-29

On-Brand Devices [CROSSTRAC]

• 00885554022223: MTO ASSEMBLY BULLET CROSSTRAC II
• 00885554022216: MTO ASSEMBLY HIP GUIDE CROSSTRAC II
• 03596010610270: TRAY CROSSTRAC
• 03596010610263: CROSSTRAC HIP GUIDE BULLET
• 03596010610256: CROSSTRAC HIP GUIDE