gudid Primary ID: MFS-96000BQ

MEIDIKE GENE (UDI MFS-96000BQ)

Manufactured by MEDICO TECHNOLOGY CO., LTD

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

Scannable UDI-DI Representation

Device Regulatory Overview

The MEIDIKE GENE (Model/Catalog Number: MFS-96000BQ) is a medical device manufactured by MEDICO TECHNOLOGY CO., LTD. This product is indexed under FDA Product Code / Category Classification KXG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: MFS-96000BQ
Product Code / EMDN: KXG
Device Name
Database Sync Date: 2026-08-09 09:06:36

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 MEIDIKE GENE?

The registered manufacturer of record for MEIDIKE GENE is MEDICO TECHNOLOGY CO., LTD.

What is the Primary UDI-DI identifier for MEIDIKE GENE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MFS-96000BQ.

What classification code is assigned to this device?

This device is registered under product classification code KXG.

Similar Classification Devices (KXG)

Other Devices by MEDICO TECHNOLOGY CO., LTD

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