gudid Primary ID: CT+

Imex CT+ Doppler (UDI CT+)

Manufactured by IMEX, LLC

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Imex CT+ Doppler (Model/Catalog Number: CT+) is a medical device manufactured by IMEX, LLC. This product is indexed under FDA Product Code / Category Classification JAF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: CT+
Product Code / EMDN: JAF
Device Name: Imex CT+ Doppler system main unit
Database Sync Date: 2026-08-09 09:49:16

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 Imex CT+ Doppler?

The registered manufacturer of record for Imex CT+ Doppler is IMEX, LLC.

What is the Primary UDI-DI identifier for Imex CT+ Doppler?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CT+.

What classification code is assigned to this device?

This device is registered under product classification code JAF.

Similar Classification Devices (JAF)

Other Devices by IMEX, LLC

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