gudid Primary ID: 2010400

MicroPort (UDI 2010400)

Manufactured by Apex (Guangzhou) Tools & Orthopedics Co.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The MicroPort (Model/Catalog Number: 2010400) is a medical device manufactured by Apex (Guangzhou) Tools & Orthopedics Co.. This product is indexed under FDA Product Code / Category Classification FQH within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 2010400
Product Code / EMDN: FQH
Device Name: HIP KIT
Database Sync Date: 2026-08-09 09:05:24

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 MicroPort?

The registered manufacturer of record for MicroPort is Apex (Guangzhou) Tools & Orthopedics Co..

What is the Primary UDI-DI identifier for MicroPort?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2010400.

What classification code is assigned to this device?

This device is registered under product classification code FQH.

Similar Classification Devices (FQH)

Other Devices by Apex (Guangzhou) Tools & Orthopedics Co.

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