gudid Primary ID: DECC066380

EliA GliadinDP IgA Well (UDI DECC066380)

Manufactured by Phadia AB

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The EliA GliadinDP IgA Well (Model/Catalog Number: DECC066380) is a medical device manufactured by Phadia AB. This product is indexed under FDA Product Code / Category Classification MST within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: DECC066380
Product Code / EMDN: MST
Device Name: EliA GliadinDP IgA Well
Database Sync Date: 2026-08-09 09:48:59

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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Frequently Asked Questions

Who is the primary manufacturer of EliA GliadinDP IgA Well?

The registered manufacturer of record for EliA GliadinDP IgA Well is Phadia AB.

What is the Primary UDI-DI identifier for EliA GliadinDP IgA Well?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DECC066380.

What classification code is assigned to this device?

This device is registered under product classification code MST.

Similar Classification Devices (MST)

Other Devices by Phadia AB

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