GUDIDData
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eudamed_udi Primary ID: 05901292108243

Rurka tracheostomijna bez mankietu (UDI 05901292108243)

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 tracheostomijna bez mankietu - Primary ID 05901292108243

Device Regulatory Overview

The Rurka tracheostomijna bez mankietu (Model/Catalog Number: 33-5052) is a medical device manufactured by SUMI spółka z ograniczoną odpowiedzialnością spółka komandytowa. This product is indexed under FDA Product Code / Category Classification R0105010101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
33-5052
Product Code / EMDN
R0105010101
Device Name
Rurka tracheostomijna bez mankietu
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 Rurka tracheostomijna bez mankietu?

The registered manufacturer of record for Rurka tracheostomijna bez mankietu is SUMI spółka z ograniczoną odpowiedzialnością spółka komandytowa.

What is the Primary UDI-DI identifier for Rurka tracheostomijna bez mankietu?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05901292108243.

What classification code is assigned to this device?

This device is registered under product classification code R0105010101.

Similar Classification Devices (R0105010101)

Other Devices by SUMI spółka z ograniczoną odpowiedzialnością spółka komandytowa

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