FDP (eCLIA) (UDI 06975984064246)
Manufactured by Shenzhen Lifotronic Technology Co., Ltd.
Device Regulatory Overview
The FDP (eCLIA) (Model/Catalog Number: 0320510204) is a medical device manufactured by Shenzhen Lifotronic Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0103020502 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0320510204
- Product Code / EMDN
- W0103020502
- Device Name
- FDP (eCLIA)
- Database Sync Date
- 2026-08-09 18:39:09
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 FDP (eCLIA)?
The registered manufacturer of record for FDP (eCLIA) is Shenzhen Lifotronic Technology Co., Ltd..
What is the Primary UDI-DI identifier for FDP (eCLIA)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975984064246.
What classification code is assigned to this device?
This device is registered under product classification code W0103020502.
Similar Classification Devices (W0103020502)
Other Devices by Shenzhen Lifotronic Technology Co., Ltd.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint