gudid Primary ID: DECC055980

EliA Ro52 Well (UDI DECC055980)

Manufactured by Phadia AB

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

Scannable UDI-DI Representation

Device Regulatory Overview

The EliA Ro52 Well (Model/Catalog Number: DECC055980) is a medical device manufactured by Phadia AB. This product is indexed under FDA Product Code / Category Classification LKJ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: DECC055980
Product Code / EMDN: LKJ
Device Name: EliA Ro52 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 Ro52 Well?

The registered manufacturer of record for EliA Ro52 Well is Phadia AB.

What is the Primary UDI-DI identifier for EliA Ro52 Well?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DECC055980.

What classification code is assigned to this device?

This device is registered under product classification code LKJ.

Similar Classification Devices (LKJ)

Other Devices by Phadia AB

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