gudid Primary ID: ME-2309D

Flush Solution (UDI ME-2309D)

Manufactured by Diamond Diagnostics Inc.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Flush Solution (Model/Catalog Number: ME-2309D) is a medical device manufactured by Diamond Diagnostics Inc.. This product is indexed under FDA Product Code / Category Classification CGZ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: ME-2309D
Product Code / EMDN: CGZ
Device Name
Database Sync Date: 2026-08-09 09:22:15

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 Flush Solution?

The registered manufacturer of record for Flush Solution is Diamond Diagnostics Inc..

What is the Primary UDI-DI identifier for Flush Solution?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ME-2309D.

What classification code is assigned to this device?

This device is registered under product classification code CGZ.

Similar Classification Devices (CGZ)

Other Devices by Diamond Diagnostics Inc.

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