eudamed_udi Primary ID: 05901292126841

Kaniula wewnętrzna (UDI 05901292126841)

Manufactured by SUMI spółka z ograniczoną odpowiedzialnością spółka komandytowa

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Kaniula wewnętrzna (Model/Catalog Number: 45-9001) is a medical device manufactured by SUMI spółka z ograniczoną odpowiedzialnością spółka komandytowa. This product is indexed under FDA Product Code / Category Classification R010503 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 45-9001
Product Code / EMDN: R010503
Device Name: Tracheostomijna kaniula wewnętrzna
Database Sync Date: 2026-08-09 16:45:08

Full Regulatory Attributes

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{
    "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 Kaniula wewnętrzna?

The registered manufacturer of record for Kaniula wewnętrzna is SUMI spółka z ograniczoną odpowiedzialnością spółka komandytowa.

What is the Primary UDI-DI identifier for Kaniula wewnętrzna?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05901292126841.

What classification code is assigned to this device?

This device is registered under product classification code R010503.

Similar Classification Devices (R010503)

Other Devices by SUMI spółka z ograniczoną odpowiedzialnością spółka komandytowa

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