GUDIDData
eudamed_udi Primary ID: 04542187215540

ReadiCath All Silicone Reusable Catheter Set ・Female Type (UDI 04542187215540)

Manufactured by CREATE MEDIC CO., LTD.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ReadiCath All Silicone Reusable Catheter Set ・Female Type - Primary ID 04542187215540

Device Regulatory Overview

The ReadiCath All Silicone Reusable Catheter Set ・Female Type (Model/Catalog Number: 04-4114H) is a medical device manufactured by CREATE MEDIC CO., LTD.. This product is indexed under FDA Product Code / Category Classification U010199 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
04-4114H
Product Code / EMDN
U010199
Device Name
Self-Catheterization Set
Database Sync Date
2026-08-09 16:50:46

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 ReadiCath All Silicone Reusable Catheter Set ・Female Type?

The registered manufacturer of record for ReadiCath All Silicone Reusable Catheter Set ・Female Type is CREATE MEDIC CO., LTD..

What is the Primary UDI-DI identifier for ReadiCath All Silicone Reusable Catheter Set ・Female Type?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04542187215540.

What classification code is assigned to this device?

This device is registered under product classification code U010199.

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