THOR Anterior Plating System 48031500

GUDID 07613327262834

ANTI-TORQUE KEY

Stryker Corporation

Orthopaedic counter-torque/rod-pushing instrument

• Primary Device ID: 07613327262834
• NIH Device Record Key: 2ecc8ebd-2fae-41b5-9c20-be1b08a4b279
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: THOR Anterior Plating System
• Version Model Number: 48031500
• Catalog Number: 48031500
• Company DUNS: 149183167
• Company Name: Stryker Corporation
• 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: true
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	07613327262834 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[07613327262834]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-11-11
• Device Publish Date: 2018-09-24

On-Brand Devices [THOR Anterior Plating System]

• 07613327262834: ANTI-TORQUE KEY
• 07613327262803: SCREWDRIVER SHAFT
• 07613327262797: TORQUE WRENCH SOCKET
• 07613327262766: UNIVERSAL SCREWDRIVER SHAFT