gudid
Primary ID: EOS Plus
ADS (UDI EOS Plus)
Manufactured by Guangzhou Ajax Medical Equipment Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ADS - Primary ID EOS Plus
Device Regulatory Overview
The ADS (Model/Catalog Number: EOS Plus) is a medical device manufactured by Guangzhou Ajax Medical Equipment Co., Ltd.. This product is indexed under FDA Product Code / Category Classification FRA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- EOS Plus
- Product Code / EMDN
- FRA
- Device Name
- Database Sync Date
- 2026-08-09 09:06:43
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 ADS?
The registered manufacturer of record for ADS is Guangzhou Ajax Medical Equipment Co., Ltd..
What is the Primary UDI-DI identifier for ADS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is EOS Plus.
What classification code is assigned to this device?
This device is registered under product classification code FRA.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint