gudid
Primary ID: C525-60
Teco Diagnostics Carbon Dioxide (CO2) Reagent Set (UDI C525-60)
Manufactured by TECO DIAGNOSTICS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Teco Diagnostics Carbon Dioxide (CO2) Reagent Set - Primary ID C525-60
Device Regulatory Overview
The Teco Diagnostics Carbon Dioxide (CO2) Reagent Set (Model/Catalog Number: C525-60) is a medical device manufactured by TECO DIAGNOSTICS. This product is indexed under FDA Product Code / Category Classification KHS within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- C525-60
- Product Code / EMDN
- KHS
- Device Name
- Teco Diagnostics Carbon Dioxide (CO2) Reagent Set is used for manual or automated quantitative determination of carbon dioxide content in human plasma or serum at 340 nm.
- 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 Carbon Dioxide (CO2) Reagent Set?
The registered manufacturer of record for Teco Diagnostics Carbon Dioxide (CO2) Reagent Set is TECO DIAGNOSTICS.
What is the Primary UDI-DI identifier for Teco Diagnostics Carbon Dioxide (CO2) Reagent Set?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is C525-60.
What classification code is assigned to this device?
This device is registered under product classification code KHS.
Similar Classification Devices (KHS)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint