GUDIDData
eudamed_udi Primary ID: 05901292105525

Rurka dooskrzelowa prawostronna (UDI 05901292105525)

Manufactured by SUMI spółka z ograniczoną odpowiedzialnością spółka komandytowa

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Rurka dooskrzelowa prawostronna - Primary ID 05901292105525

Device Regulatory Overview

The Rurka dooskrzelowa prawostronna (Model/Catalog Number: 22-7010) is a medical device manufactured by SUMI spółka z ograniczoną odpowiedzialnością spółka komandytowa. This product is indexed under FDA Product Code / Category Classification R010499 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
22-7010
Product Code / EMDN
R010499
Device Name
Rurka dooskrzelowa prawostronna
Database Sync Date
2026-08-09 16:28:53

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 Rurka dooskrzelowa prawostronna?

The registered manufacturer of record for Rurka dooskrzelowa prawostronna is SUMI spółka z ograniczoną odpowiedzialnością spółka komandytowa.

What is the Primary UDI-DI identifier for Rurka dooskrzelowa prawostronna?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05901292105525.

What classification code is assigned to this device?

This device is registered under product classification code R010499.

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