gudid Primary ID: FDP-8

FDP Probe (UDI FDP-8)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The FDP Probe (Model/Catalog Number: FDP-8) is a medical device manufactured by KOVEN TECHNOLOGY, INC.. This product is indexed under FDA Product Code / Category Classification JAF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: FDP-8
Product Code / EMDN: JAF
Device Name: Flat PW Doppler probe, 8 MHz
Database Sync Date: 2026-08-09 09:46:58

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 FDP Probe?

The registered manufacturer of record for FDP Probe is KOVEN TECHNOLOGY, INC..

What is the Primary UDI-DI identifier for FDP Probe?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FDP-8.

What classification code is assigned to this device?

This device is registered under product classification code JAF.

Similar Classification Devices (JAF)

Other Devices by KOVEN TECHNOLOGY, INC.

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