eudamed_udi Primary ID: 08800027300723

MDK HANDPIECES (UDI 08800027300723)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The MDK HANDPIECES (Model/Catalog Number: MOKO 250B) is a medical device manufactured by MDK CO., LTD.. This product is indexed under FDA Product Code / Category Classification L15900699 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: MOKO 250B
Product Code / EMDN: L15900699
Device Name: Electrical air driven dental handpieces
Database Sync Date: 2026-08-09 18:12:43

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 MDK HANDPIECES?

The registered manufacturer of record for MDK HANDPIECES is MDK CO., LTD..

What is the Primary UDI-DI identifier for MDK HANDPIECES?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08800027300723.

What classification code is assigned to this device?

This device is registered under product classification code L15900699.

Similar Classification Devices (L15900699)

Other Devices by MDK CO., LTD.

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