390023

GUDID 37613327072724

Wire with Eye

Stryker Trauma SA

Orthopaedic bone wire

• Primary Device ID: 37613327072724
• NIH Device Record Key: 2c34fdab-2ec6-4886-a054-7c2798371382
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 390023
• Catalog Number: 390023
• Company DUNS: 481999654
• Company Name: Stryker Trauma SA
• Device Count: 10
• 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: true
• 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

Device Dimensions

• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter
• Device Size Text, specify: 0
• Length: 350 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327072723 [Unit of Use]
GS1	37613327072724 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K914374

FDA Product Code

• JDQ: CERCLAGE, FIXATION

Sterilization

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

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

[37613327072724]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-09-24

Devices Manufactured by Stryker Trauma SA

• 07613327555554 - VARIAX: 2024-10-30 T-handle, Cannulated Three-jaw Chuck
• 07613327605808 - PANGEA: 2024-10-18 Small Frag. Proximal Tibia Targeter Tray
• 07613327603101 - REUNION: 2024-10-09 Modular Glenoid Surface Trial
• 07613327603118 - REUNION: 2024-10-09 Modular Glenoid Surface Trial
• 07613327603125 - REUNION: 2024-10-09 Modular Glenoid Surface Trial
• 07613327603132 - REUNION: 2024-10-09 Modular Humeral Head Trial
• 07613327603149 - REUNION: 2024-10-09 Modular Glenoid Surface Trial
• 07613327603156 - REUNION: 2024-10-09 Modular Humeral Head Trial