gudid
Primary ID: 210-01
AWI (UDI 210-01)
Manufactured by Apex (Guangzhou) Tools & Orthopedics Co.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AWI - Primary ID 210-01
Device Regulatory Overview
The AWI (Model/Catalog Number: 210-01) is a medical device manufactured by Apex (Guangzhou) Tools & Orthopedics Co.. This product is indexed under FDA Product Code / Category Classification FON within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 210-01
- Product Code / EMDN
- FON
- Device Name
- EXTREMITY IRRIGATION BAG
- Database Sync Date
- 2026-08-09 09:05:24
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)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 210-01.
What classification code is assigned to this device?
This device is registered under product classification code FON.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint