RTK10531 OR Turnover Kit RTK10531

GUDID 20787551040337

RTK10531 OR Turnover Kit

XODUS MEDICAL, INC.

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• Primary Device ID: 20787551040337
• NIH Device Record Key: c3044208-c537-4da0-be93-a627f2105f58
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RTK10531 OR Turnover Kit
• Version Model Number: RTK10531
• Catalog Number: RTK10531
• Company DUNS: 868042664
• Company Name: XODUS MEDICAL, 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: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com
• Phone: +1(724)337-5500
• Email: plloyd@xodusmedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00787551040333 [Primary]
GS1	20787551040337 [Package]; Contains: 00787551040333; Package: CASE [18 Units]; In Commercial Distribution

FDA Product Code

• KDD: Kit, surgical instrument, disposable

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-11-03
• Device Publish Date: 2023-10-26

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