Automated CLEIA system (UDI 06980222380019)
Manufactured by Chengdu Illumaxbio Technology Co.,LTD
Device Regulatory Overview
The Automated CLEIA system (Model/Catalog Number: E101) is a medical device manufactured by Chengdu Illumaxbio Technology Co.,LTD. This product is indexed under FDA Product Code / Category Classification W0201020101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- E101
- Product Code / EMDN
- W0201020101
- Device Name
- Automated CLEIA system
- Database Sync Date
- 2026-08-09 16:46:17
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 Automated CLEIA system?
The registered manufacturer of record for Automated CLEIA system is Chengdu Illumaxbio Technology Co.,LTD.
What is the Primary UDI-DI identifier for Automated CLEIA system?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06980222380019.
What classification code is assigned to this device?
This device is registered under product classification code W0201020101.
Similar Classification Devices (W0201020101)
Other Devices by Chengdu Illumaxbio Technology Co.,LTD
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint