GUDIDData
gudid Primary ID: G22218

Marcon (UDI G22218)

Manufactured by COOK IRELAND LTD

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Marcon - Primary ID G22218

Device Regulatory Overview

The Marcon (Model/Catalog Number: G22218) is a medical device manufactured by COOK IRELAND LTD. This product is indexed under FDA Product Code / Category Classification FEG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
G22218
Product Code / EMDN
FEG
Device Name
Marcon Colon Decompression Set
Database Sync Date
2026-08-09 09:33:21

Full Regulatory Attributes

🔒 Token Gated
{
    "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 Marcon?

The registered manufacturer of record for Marcon is COOK IRELAND LTD.

What is the Primary UDI-DI identifier for Marcon?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G22218.

What classification code is assigned to this device?

This device is registered under product classification code FEG.

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