Teco Diagnostics LDH Liquid Reagent Kit for TC Matrix (UDI L533-780TC2)
Manufactured by TECO DIAGNOSTICS
Device Regulatory Overview
The Teco Diagnostics LDH Liquid Reagent Kit for TC Matrix (Model/Catalog Number: L533-780TC2) is a medical device manufactured by TECO DIAGNOSTICS. This product is indexed under FDA Product Code / Category Classification CFJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- L533-780TC2
- Product Code / EMDN
- CFJ
- Device Name
- Teco Diagnostics LDH Liquid Reagent Kit for TC Matrix is for the quantitative determination of lactate dehydrogenase activity in serum or plasma on TC Matrix analyzers.
- Database Sync Date
- 2026-08-09 10:01:14
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Teco Diagnostics LDH Liquid Reagent Kit for TC Matrix?
The registered manufacturer of record for Teco Diagnostics LDH Liquid Reagent Kit for TC Matrix is TECO DIAGNOSTICS.
What is the Primary UDI-DI identifier for Teco Diagnostics LDH Liquid Reagent Kit for TC Matrix?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is L533-780TC2.
What classification code is assigned to this device?
This device is registered under product classification code CFJ.
Similar Classification Devices (CFJ)
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