eudamed_udi Primary ID: G520MD28000

Amalgam Carrier Double End (UDI G520MD28000)

Manufactured by Medspo

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Amalgam Carrier Double End (Model/Catalog Number: MD2800) is a medical device manufactured by Medspo. This product is indexed under FDA Product Code / Category Classification Q01010199 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: MD2800
Product Code / EMDN: Q01010199
Device Name: Amalgam Carrier Double End
Database Sync Date: 2026-08-09 16:50:53

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 Amalgam Carrier Double End?

The registered manufacturer of record for Amalgam Carrier Double End is Medspo.

What is the Primary UDI-DI identifier for Amalgam Carrier Double End?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G520MD28000.

What classification code is assigned to this device?

This device is registered under product classification code Q01010199.

Similar Classification Devices (Q01010199)

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