eudamed_udi Primary ID: 05901292138585

Rurka tracheostomijna z mankietem (UDI 05901292138585)

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 Rurka tracheostomijna z mankietem (Model/Catalog Number: 35-8018) is a medical device manufactured by SUMI spółka z ograniczoną odpowiedzialnością spółka komandytowa. This product is indexed under FDA Product Code / Category Classification R0105020102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 35-8018
Product Code / EMDN: R0105020102
Device Name: Rurka tracheostomijna z mankietem
Database Sync Date: 2026-08-09 16:29:36

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 Rurka tracheostomijna z mankietem?

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

What is the Primary UDI-DI identifier for Rurka tracheostomijna z mankietem?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05901292138585.

What classification code is assigned to this device?

This device is registered under product classification code R0105020102.

Similar Classification Devices (R0105020102)

Other Devices by SUMI spółka z ograniczoną odpowiedzialnością spółka komandytowa

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