FDP Assay kit CLIA (UDI 06974521004097)
Manufactured by Shenzhen Superbio Technology Co.,Ltd.
Device Regulatory Overview
The FDP Assay kit CLIA (Model/Catalog Number: SUPM084072) is a medical device manufactured by Shenzhen Superbio 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
- SUPM084072
- Product Code / EMDN
- W0103020502
- Device Name
- FDP Assay kit CLIA
- Database Sync Date
- 2026-08-09 18:09:25
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 Assay kit CLIA?
The registered manufacturer of record for FDP Assay kit CLIA is Shenzhen Superbio Technology Co.,Ltd..
What is the Primary UDI-DI identifier for FDP Assay kit CLIA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974521004097.
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 Superbio Technology Co.,Ltd.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint