Teco Diagnostics Hemoglobin A1c Set for TC Matrix Systems (UDI G560-160TM)
Manufactured by TECO DIAGNOSTICS
Device Regulatory Overview
The Teco Diagnostics Hemoglobin A1c Set for TC Matrix Systems (Model/Catalog Number: G560-160TM) is a medical device manufactured by TECO DIAGNOSTICS. This product is indexed under FDA Product Code / Category Classification LCP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- G560-160TM
- Product Code / EMDN
- LCP
- Device Name
- Teco Diagnostics Hemoglobin A1c Set for TC Matrix Systems is used for the quantitative determination of Hemoglobin A1c (HbA1c) in human blood 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 Hemoglobin A1c Set for TC Matrix Systems?
The registered manufacturer of record for Teco Diagnostics Hemoglobin A1c Set for TC Matrix Systems is TECO DIAGNOSTICS.
What is the Primary UDI-DI identifier for Teco Diagnostics Hemoglobin A1c Set for TC Matrix Systems?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G560-160TM.
What classification code is assigned to this device?
This device is registered under product classification code LCP.
Similar Classification Devices (LCP)
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