GUDIDData
eudamed_udi Primary ID: 05904553993824

Extension tubing for infusion pump (UDI 05904553993824)

Manufactured by MARGOMED SPÓŁKA AKCYJNA

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Extension tubing for infusion pump - Primary ID 05904553993824

Device Regulatory Overview

The Extension tubing for infusion pump (Model/Catalog Number: 004 220) is a medical device manufactured by MARGOMED SPÓŁKA AKCYJNA. This product is indexed under FDA Product Code / Category Classification A03020199 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
004 220
Product Code / EMDN
A03020199
Device Name
Extension tubing
Database Sync Date
2026-08-09 17:20:56

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 Extension tubing for infusion pump?

The registered manufacturer of record for Extension tubing for infusion pump is MARGOMED SPÓŁKA AKCYJNA.

What is the Primary UDI-DI identifier for Extension tubing for infusion pump?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05904553993824.

What classification code is assigned to this device?

This device is registered under product classification code A03020199.

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