gudid Primary ID: 209-06

AWI (UDI 209-06)

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 AWI (Model/Catalog Number: 209-06) 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: 209-06
Product Code / EMDN: FQH
Device Name: TRUNK-L IRRIGATION 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 AWI?

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

What is the Primary UDI-DI identifier for AWI?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 209-06.

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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