eudamed_udi Primary ID: D-CGI0197K

Corgi® (UDI D-CGI0197K)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Corgi® (Model/Catalog Number: CGI019) is a medical device manufactured by Phantom Laboratory. This product is indexed under FDA Product Code / Category Classification Z119080 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: CGI019
Product Code / EMDN: Z119080
Device Name: CGI019
Database Sync Date: 2026-08-09 16:51:18

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 Corgi®?

The registered manufacturer of record for Corgi® is Phantom Laboratory.

What is the Primary UDI-DI identifier for Corgi®?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-CGI0197K.

What classification code is assigned to this device?

This device is registered under product classification code Z119080.

Similar Classification Devices (Z119080)

Other Devices by Phantom Laboratory

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