gudid Primary ID: DTF-38

Trigger-Flex (UDI DTF-38)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Trigger-Flex (Model/Catalog Number: DTF-38) is a medical device manufactured by ELLIQUENCE, LLC. This product is indexed under FDA Product Code / Category Classification GEI within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: DTF-38
Product Code / EMDN: GEI
Device Name: A2E 38cm
Database Sync Date: 2026-08-09 09:21:00

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of Trigger-Flex?

The registered manufacturer of record for Trigger-Flex is ELLIQUENCE, LLC.

What is the Primary UDI-DI identifier for Trigger-Flex?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DTF-38.

What classification code is assigned to this device?

This device is registered under product classification code GEI.

Similar Classification Devices (GEI)

Other Devices by ELLIQUENCE, LLC

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