GUDIDData
eudamed_udi Primary ID: 05904553993374

Infusion set IS with injection site (UDI 05904553993374)

Manufactured by MARGOMED SPÓŁKA AKCYJNA

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Infusion set IS with injection site - Primary ID 05904553993374

Device Regulatory Overview

The Infusion set IS with injection site (Model/Catalog Number: 001 455) is a medical device manufactured by MARGOMED SPÓŁKA AKCYJNA. This product is indexed under FDA Product Code / Category Classification A03040199 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
001 455
Product Code / EMDN
A03040199
Device Name
Infusion Set
Database Sync Date
2026-08-09 16:49:24

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 Infusion set IS with injection site?

The registered manufacturer of record for Infusion set IS with injection site is MARGOMED SPÓŁKA AKCYJNA.

What is the Primary UDI-DI identifier for Infusion set IS with injection site?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05904553993374.

What classification code is assigned to this device?

This device is registered under product classification code A03040199.

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