gudid
Primary ID: UW600-III
NA (UDI UW600-III)
Manufactured by Hangzhou AGS MedTech Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NA - Primary ID UW600-III
Device Regulatory Overview
The NA (Model/Catalog Number: UW600-III) is a medical device manufactured by Hangzhou AGS MedTech Co., Ltd.. This product is indexed under FDA Product Code / Category Classification OCX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- UW600-III
- Product Code / EMDN
- OCX
- Device Name
- Database Sync Date
- 2026-08-09 09:05:22
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 NA?
The registered manufacturer of record for NA is Hangzhou AGS MedTech Co., Ltd..
What is the Primary UDI-DI identifier for NA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is UW600-III.
What classification code is assigned to this device?
This device is registered under product classification code OCX.
Similar Classification Devices (OCX)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint