GUDIDData
eudamed_udi Primary ID: 05907996831913

dicoNEX Single use syringe, 3-part (UDI 05907996831913)

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 syringe, 3-part - Primary ID 05907996831913

Device Regulatory Overview

The dicoNEX Single use syringe, 3-part (Model/Catalog Number: 001ML-3CZ-BL) is a medical device manufactured by ZARYS International Spółka z ograniczoną odpowiedzialnością. This product is indexed under FDA Product Code / Category Classification A020102010202 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
001ML-3CZ-BL
Product Code / EMDN
A020102010202
Device Name
sterile syringe
Database Sync Date
2026-08-09 16:29:08

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 syringe, 3-part?

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

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05907996831913.

What classification code is assigned to this device?

This device is registered under product classification code A020102010202.

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