Trigger-Flex®

GUDID 00846338001223

ELLIQUENCE, LLC

Endoscopic electrosurgical handpiece/electrode, bipolar, single-use

• Primary Device ID: 00846338001223
• NIH Device Record Key: b8f89bb5-3f10-4040-ae3d-18ca20c66162
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Trigger-Flex®
• Version Model Number: 40990.0031
• 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	00846338001223 [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: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-04-23
• Device Publish Date: 2016-09-22

On-Brand Devices [Trigger-Flex®]

• 00846338010713: DTF-38
• 00846338010706: DTF-35
• 00846338001223: 40990.0031
• 00846338001216: A2E 38cm
• 00846338001018: DTF-32
• 00846338000998: DTF-39
• 00846338000943: DTF-24B
• 00846338000936: DTF-13
• 00846338000851: DTF-40
• 00846338000844: M 35cm
• 00846338000837: DTF-18
• 00846338000455: 4793.692
• 00846338000288: DTF-31
• 00846338000066: S 36cm