Teco Diagnostics Lactate Dehydrogenase (LDH-L) Liquid Reagent Set (UDI L533-150)
Manufactured by TECO DIAGNOSTICS
Device Regulatory Overview
The Teco Diagnostics Lactate Dehydrogenase (LDH-L) Liquid Reagent Set (Model/Catalog Number: L533-150) 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
- L533-150
- Product Code / EMDN
- CFJ
- Device Name
- Teco Diagnostics Lactate Dehydrogenase (LDH-L) Liquid Reagent Set is for the In Vitro quantitative kinetic determination of Lactate Dehydrogenase activity in serum.
- 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 Lactate Dehydrogenase (LDH-L) Liquid Reagent Set?
The registered manufacturer of record for Teco Diagnostics Lactate Dehydrogenase (LDH-L) Liquid Reagent Set is TECO DIAGNOSTICS.
What is the Primary UDI-DI identifier for Teco Diagnostics Lactate Dehydrogenase (LDH-L) Liquid Reagent Set?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is L533-150.
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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