GUDIDData
eudamed_udi Primary ID: 05907996868087

TWO-WAY FOLEY CATHETER with plastic valve (UDI 05907996868087)

Manufactured by ZARYS International Spółka z ograniczoną odpowiedzialnością

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TWO-WAY FOLEY CATHETER with plastic valve - Primary ID 05907996868087

Device Regulatory Overview

The TWO-WAY FOLEY CATHETER with plastic valve (Model/Catalog Number: CFNSG-2D-12-10-P) is a medical device manufactured by ZARYS International Spółka z ograniczoną odpowiedzialnością. This product is indexed under FDA Product Code / Category Classification U010201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
CFNSG-2D-12-10-P
Product Code / EMDN
U010201
Device Name
sterile Foley catheter
Database Sync Date
2026-08-09 16:46:09

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 TWO-WAY FOLEY CATHETER with plastic valve?

The registered manufacturer of record for TWO-WAY FOLEY CATHETER with plastic valve is ZARYS International Spółka z ograniczoną odpowiedzialnością.

What is the Primary UDI-DI identifier for TWO-WAY FOLEY CATHETER with plastic valve?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05907996868087.

What classification code is assigned to this device?

This device is registered under product classification code U010201.

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