GUDIDData
eudamed_udi Primary ID: 05906395982943

Nasadka zimowa ø18 (UDI 05906395982943)

Manufactured by MIKIRAD Spółka z ograniczona odpowiedzialnością

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Nasadka zimowa ø18 - Primary ID 05906395982943

Device Regulatory Overview

The Nasadka zimowa ø18 (Model/Catalog Number: 13/MR.Z ø18) is a medical device manufactured by MIKIRAD Spółka z ograniczona odpowiedzialnością. This product is indexed under FDA Product Code / Category Classification Y120380 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
13/MR.Z ø18
Product Code / EMDN
Y120380
Device Name
NASADKA UNIWERSALNA
Database Sync Date
2026-08-09 16:45:41

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 Nasadka zimowa ø18?

The registered manufacturer of record for Nasadka zimowa ø18 is MIKIRAD Spółka z ograniczona odpowiedzialnością.

What is the Primary UDI-DI identifier for Nasadka zimowa ø18?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05906395982943.

What classification code is assigned to this device?

This device is registered under product classification code Y120380.

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