GUDIDData
eudamed_udi Primary ID: 00810164510280

Fluorescence Immunoasasy Analyzer (UDI 00810164510280)

Manufactured by Aceso Laboratories, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Fluorescence Immunoasasy Analyzer - Primary ID 00810164510280

Device Regulatory Overview

The Fluorescence Immunoasasy Analyzer (Model/Catalog Number: EQB01-FI) is a medical device manufactured by Aceso Laboratories, Inc.. This product is indexed under FDA Product Code / Category Classification W0201020201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
EQB01-FI
Product Code / EMDN
W0201020201
Device Name
Fluorescence Immunoasasy Analyzer
Database Sync Date
2026-08-09 16:47:01

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 Fluorescence Immunoasasy Analyzer?

The registered manufacturer of record for Fluorescence Immunoasasy Analyzer is Aceso Laboratories, Inc..

What is the Primary UDI-DI identifier for Fluorescence Immunoasasy Analyzer?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00810164510280.

What classification code is assigned to this device?

This device is registered under product classification code W0201020201.

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