GUDIDData
gudid Primary ID: ASO-100

Teco Diagnostics Anti-Streptolysin O (ASO) Reagent Set (UDI ASO-100)

Manufactured by TECO DIAGNOSTICS

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Teco Diagnostics Anti-Streptolysin O (ASO) Reagent Set - Primary ID ASO-100

Device Regulatory Overview

The Teco Diagnostics Anti-Streptolysin O (ASO) Reagent Set (Model/Catalog Number: ASO-100) is a medical device manufactured by TECO DIAGNOSTICS. This product is indexed under FDA Product Code / Category Classification GTQ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
ASO-100
Product Code / EMDN
GTQ
Device Name
Teco Diagnostics Anti-Streptolysin O (ASO) Reagent Set is for the qualitative and semi-quantitative measurement of antibodies to streptococcal exoenzymes in human serum.
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
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Teco Diagnostics Anti-Streptolysin O (ASO) Reagent Set?

The registered manufacturer of record for Teco Diagnostics Anti-Streptolysin O (ASO) Reagent Set is TECO DIAGNOSTICS.

What is the Primary UDI-DI identifier for Teco Diagnostics Anti-Streptolysin O (ASO) Reagent Set?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ASO-100.

What classification code is assigned to this device?

This device is registered under product classification code GTQ.

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