Screw Removal Tool

GUDID 00810028395060

Trilliant Surgical, LLC

Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable Orthopaedic implant inserter/extractor, reusable

• Primary Device ID: 00810028395060
• NIH Device Record Key: e5ae08ee-4868-4177-9e65-3c0b3b0c696d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Screw Removal Tool
• Version Model Number: 211-00-006
• 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	00810028395060 [Primary]

FDA Product Code

• HWB: Extractor

Sterilization

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

[00810028395060]

Moist Heat or Steam Sterilization

[00810028395060]

Moist Heat or Steam Sterilization

[00810028395060]

Moist Heat or Steam Sterilization

[00810028395060]

Moist Heat or Steam Sterilization

[00810028395060]

Moist Heat or Steam Sterilization

[00810028395060]

Moist Heat or Steam Sterilization

[00810028395060]

Moist Heat or Steam Sterilization

[00810028395060]

Moist Heat or Steam Sterilization

[00810028395060]

Moist Heat or Steam Sterilization

[00810028395060]

Moist Heat or Steam Sterilization

[00810028395060]

Moist Heat or Steam Sterilization

[00810028395060]

Moist Heat or Steam Sterilization

[00810028395060]

Moist Heat or Steam Sterilization

[00810028395060]

Moist Heat or Steam Sterilization

[00810028395060]

Moist Heat or Steam Sterilization

[00810028395060]

Moist Heat or Steam Sterilization

[00810028395060]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-03-29
• Device Publish Date: 2024-03-21

Devices Manufactured by Trilliant Surgical, LLC

• 00810028395343 - Revision MTP Plate, L, 0°: 2024-04-04
• 00810028394995 - Cannulated Depth Gauge: 2024-03-29
• 00810028395022 - 2.0/2.4 Cannulated Driver Bit: 2024-03-29
• 00810028395039 - 3.0/4.0 Cannulated Driver: 2024-03-29
• 00810028395046 - 2.0/2.4 Removal Tool: 2024-03-29
• 00810028395053 - 3.0/4.0 Removal Bit: 2024-03-29
• 00810028395060 - Screw Removal Tool: 2024-03-29
• 00810028395060 - Screw Removal Tool: 2024-03-29
• 00810028395145 - 5" K-Wire Tube, Double Ended: 2024-03-29