gudid Primary ID: T800

Imex 8MHZ DOPPLER PROBE, PD2 (UDI T800)

Manufactured by IMEX, LLC

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Imex 8MHZ DOPPLER PROBE, PD2 (Model/Catalog Number: T800) is a medical device manufactured by IMEX, LLC. This product is indexed under FDA Product Code / Category Classification KNG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: T800
Product Code / EMDN: KNG
Device Name: Imex 8MHZ DOPPLER PROBE, PD2
Database Sync Date: 2026-08-09 09:37:38

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 8MHZ DOPPLER PROBE, PD2?

The registered manufacturer of record for Imex 8MHZ DOPPLER PROBE, PD2 is IMEX, LLC.

What is the Primary UDI-DI identifier for Imex 8MHZ DOPPLER PROBE, PD2?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is T800.

What classification code is assigned to this device?

This device is registered under product classification code KNG.

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