GUDIDData
eudamed_udi Primary ID: 04542187250312

Transanálny dekompresný set na riešenie črevnej nepriechodnosti (UDI 04542187250312)

Manufactured by CREATE MEDIC CO., LTD.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Transanálny dekompresný set na riešenie črevnej nepriechodnosti - Primary ID 04542187250312

Device Regulatory Overview

The Transanálny dekompresný set na riešenie črevnej nepriechodnosti (Model/Catalog Number: 002-380-0220) is a medical device manufactured by CREATE MEDIC CO., LTD.. This product is indexed under FDA Product Code / Category Classification G0301010501 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
002-380-0220
Product Code / EMDN
G0301010501
Device Name
Transanal Ileus Decompression Tube Set
Database Sync Date
2026-08-09 16:49:18

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 Transanálny dekompresný set na riešenie črevnej nepriechodnosti?

The registered manufacturer of record for Transanálny dekompresný set na riešenie črevnej nepriechodnosti is CREATE MEDIC CO., LTD..

What is the Primary UDI-DI identifier for Transanálny dekompresný set na riešenie črevnej nepriechodnosti?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04542187250312.

What classification code is assigned to this device?

This device is registered under product classification code G0301010501.

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