gudid Primary ID: DECC055000

EliA dsDNA Well (UDI DECC055000)

Manufactured by Phadia AB

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

Scannable UDI-DI Representation

Device Regulatory Overview

The EliA dsDNA Well (Model/Catalog Number: DECC055000) is a medical device manufactured by Phadia AB. This product is indexed under FDA Product Code / Category Classification LSW within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: DECC055000
Product Code / EMDN: LSW
Device Name: EliA dsDNA 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 dsDNA Well?

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

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DECC055000.

What classification code is assigned to this device?

This device is registered under product classification code LSW.

Similar Classification Devices (LSW)

Other Devices by Phadia AB

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