Teco Diagnostics Uric Acid Liquid Reagent Kit TC-Matrix-240 (UDI U582-1170TC2)
Manufactured by TECO DIAGNOSTICS
Device Regulatory Overview
The Teco Diagnostics Uric Acid Liquid Reagent Kit TC-Matrix-240 (Model/Catalog Number: U582-1170TC2) is a medical device manufactured by TECO DIAGNOSTICS. This product is indexed under FDA Product Code / Category Classification KNK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- U582-1170TC2
- Product Code / EMDN
- KNK
- Device Name
- Teco Diagnostics Uric Acid Liquid Reagent Kit TC-Matrix-240 is used for the quantitative determination of uric acid in serum or plasma on the TC-Matrix-240 analyzer.
- Database Sync Date
- 2026-08-09 10:01:14
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 Teco Diagnostics Uric Acid Liquid Reagent Kit TC-Matrix-240?
The registered manufacturer of record for Teco Diagnostics Uric Acid Liquid Reagent Kit TC-Matrix-240 is TECO DIAGNOSTICS.
What is the Primary UDI-DI identifier for Teco Diagnostics Uric Acid Liquid Reagent Kit TC-Matrix-240?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is U582-1170TC2.
What classification code is assigned to this device?
This device is registered under product classification code KNK.
Similar Classification Devices (KNK)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint