Trigger-Flex® Quad Bipolar System

GUDID 00846338003975

ELLIQUENCE, LLC

Endoscopic electrosurgical handpiece/electrode, bipolar, single-use

• Primary Device ID: 00846338003975
• NIH Device Record Key: 890a86f6-9c20-48dd-91a7-8e89818bfe66
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Trigger-Flex® Quad Bipolar System
• Version Model Number: DTFQ-18
• Company DUNS: 019872358
• Company Name: ELLIQUENCE, LLC
• Device Count: 1
• 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: true
• 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	00846338003975 [Primary]

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-01-14
• Device Publish Date: 2025-01-06

On-Brand Devices [Trigger-Flex® Quad Bipolar System]

• 00846338001421: DTFQ-31
• 00846338003975: DTFQ-18
• 00846338004088: DTFQ-24
• 00846338003999: DTFQ-31