GUDIDData
eudamed_udi Primary ID: 05907996863525

dicoNEX Single use catheter syringe, 3-part, sterile (UDI 05907996863525)

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 dicoNEX Single use catheter syringe, 3-part, sterile - Primary ID 05907996863525

Device Regulatory Overview

The dicoNEX Single use catheter syringe, 3-part, sterile (Model/Catalog Number: 050ML-3CZ-CEW-BL) is a medical device manufactured by ZARYS International Spółka z ograniczoną odpowiedzialnością. This product is indexed under FDA Product Code / Category Classification A02010203 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
050ML-3CZ-CEW-BL
Product Code / EMDN
A02010203
Device Name
sterile catheter syringe
Database Sync Date
2026-08-09 18:44:10

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 dicoNEX Single use catheter syringe, 3-part, sterile?

The registered manufacturer of record for dicoNEX Single use catheter syringe, 3-part, sterile is ZARYS International Spółka z ograniczoną odpowiedzialnością.

What is the Primary UDI-DI identifier for dicoNEX Single use catheter syringe, 3-part, sterile?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05907996863525.

What classification code is assigned to this device?

This device is registered under product classification code A02010203.

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