gudid Primary ID: DECC066180

EliA Celikey IgG Well (UDI DECC066180)

Manufactured by Phadia AB

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

Scannable UDI-DI Representation

Device Regulatory Overview

The EliA Celikey IgG Well (Model/Catalog Number: DECC066180) is a medical device manufactured by Phadia AB. This product is indexed under FDA Product Code / Category Classification MVM within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: DECC066180
Product Code / EMDN: MVM
Device Name: EliA Celikey IgG 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 Celikey IgG Well?

The registered manufacturer of record for EliA Celikey IgG Well is Phadia AB.

What is the Primary UDI-DI identifier for EliA Celikey IgG Well?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DECC066180.

What classification code is assigned to this device?

This device is registered under product classification code MVM.

Similar Classification Devices (MVM)

Other Devices by Phadia AB

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