gudid Primary ID: DECC067000

EliA RF IgM Well (UDI DECC067000)

Manufactured by Phadia AB

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

Scannable UDI-DI Representation

Device Regulatory Overview

The EliA RF IgM Well (Model/Catalog Number: DECC067000) is a medical device manufactured by Phadia AB. This product is indexed under FDA Product Code / Category Classification DHR within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: DECC067000
Product Code / EMDN: DHR
Device Name: EliA RF IgM 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 RF IgM Well?

The registered manufacturer of record for EliA RF IgM Well is Phadia AB.

What is the Primary UDI-DI identifier for EliA RF IgM Well?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DECC067000.

What classification code is assigned to this device?

This device is registered under product classification code DHR.

Similar Classification Devices (DHR)

Other Devices by Phadia AB

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