GUDIDData
eudamed_udi Primary ID: 04542187194586

Silikon-Gastrostomie-Ersatz-Ballonzonde (Frachballon Type) mit rechtwinkliger externer Halteplatte (UDI 04542187194586)

Manufactured by CREATE MEDIC CO., LTD.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Silikon-Gastrostomie-Ersatz-Ballonzonde (Frachballon Type) mit rechtwinkliger externer Halteplatte - Primary ID 04542187194586

Device Regulatory Overview

The Silikon-Gastrostomie-Ersatz-Ballonzonde (Frachballon Type) mit rechtwinkliger externer Halteplatte (Model/Catalog Number: EN800-000-2164R) is a medical device manufactured by CREATE MEDIC CO., LTD.. This product is indexed under FDA Product Code / Category Classification G02020201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
EN800-000-2164R
Product Code / EMDN
G02020201
Device Name
All Silicone Gastrostomy Balloon Catheter
Database Sync Date
2026-08-09 17:00:05

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 Silikon-Gastrostomie-Ersatz-Ballonzonde (Frachballon Type) mit rechtwinkliger externer Halteplatte?

The registered manufacturer of record for Silikon-Gastrostomie-Ersatz-Ballonzonde (Frachballon Type) mit rechtwinkliger externer Halteplatte is CREATE MEDIC CO., LTD..

What is the Primary UDI-DI identifier for Silikon-Gastrostomie-Ersatz-Ballonzonde (Frachballon Type) mit rechtwinkliger externer Halteplatte?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04542187194586.

What classification code is assigned to this device?

This device is registered under product classification code G02020201.

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