gudid Primary ID: C-Sailor Pro

COXO (UDI C-Sailor Pro)

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: C-Sailor Pro) is a medical device manufactured by Foshan COXO Medical Instrument Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification EBW within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: C-Sailor Pro
Product Code / EMDN: EBW
Device Name: Dental Implantation Systems
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 C-Sailor Pro.

What classification code is assigned to this device?

This device is registered under product classification code EBW.

Similar Classification Devices (EBW)

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

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