Tiger Cannulated Screw System 3.0/4.0 Screw Module

GUDID 00810028397545

Trilliant Surgical, LLC

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• Primary Device ID: 00810028397545
• NIH Device Record Key: 4da7c491-4987-449a-8064-f1993b9689b0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Tiger Cannulated Screw System 3.0/4.0 Screw Module
• Version Model Number: 211-01-201
• Company DUNS: 828829072
• Company Name: Trilliant Surgical, LLC
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810028397545 [Primary]

FDA Product Code

• LRP: Tray, Surgical

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: 2024-06-12
• Device Publish Date: 2024-06-04

Devices Manufactured by Trilliant Surgical, LLC

• 00810028395008 - 2.0/2.4 Pilot Drill: 2024-06-17
• 00810028395015 - 3.0/4.0 Pilot Drill: 2024-06-17
• 00810028395077 - 2.0/2.4 Countersink: 2024-06-17
• 00810028395084 - 3.0/4.0 Countersink: 2024-06-17
• 00810028395091 - 2.0 Proximal Drill: 2024-06-17
• 00810028395107 - 2.4 Proximal Drill: 2024-06-17
• 00810028395114 - 3.0 Proximal Drill: 2024-06-17
• 00810028395121 - 4.0 Proximal Drill: 2024-06-17