COXO (UDI DB338)

Manufactured by Foshan COXO Medical Instrument Co.,Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The COXO (Model/Catalog Number: DB338) is a medical device manufactured by Foshan COXO Medical Instrument Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification EFD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: DB338
Product Code / EMDN: EFD
Device Name: Amalgamators
Database Sync Date: 2026-08-09 09:06:38

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 COXO?

The registered manufacturer of record for COXO is Foshan COXO Medical Instrument Co.,Ltd..

What is the Primary UDI-DI identifier for COXO?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DB338.

What classification code is assigned to this device?

This device is registered under product classification code EFD.

Similar Classification Devices (EFD)

Other Devices by Foshan COXO Medical Instrument Co.,Ltd.

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