eudamed_udi Primary ID: 04542187140439

Ileus Tubus (offene Spitze/einfacher Ballon) (UDI 04542187140439)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Ileus Tubus (offene Spitze/einfacher Ballon) (Model/Catalog Number: 02-45218) is a medical device manufactured by CREATE MEDIC CO., LTD.. This product is indexed under FDA Product Code / Category Classification G02020199 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 02-45218
Product Code / EMDN: G02020199
Device Name: All Silicone Ileus Tube GW Set
Database Sync Date: 2026-08-09 17:02:50

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 Ileus Tubus (offene Spitze/einfacher Ballon)?

The registered manufacturer of record for Ileus Tubus (offene Spitze/einfacher Ballon) is CREATE MEDIC CO., LTD..

What is the Primary UDI-DI identifier for Ileus Tubus (offene Spitze/einfacher Ballon)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04542187140439.

What classification code is assigned to this device?

This device is registered under product classification code G02020199.

Similar Classification Devices (G02020199)

Other Devices by CREATE MEDIC CO., LTD.

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