eudamed_udi Primary ID: 05901292104795

Rurka dooskrzelowa lewostronna (UDI 05901292104795)

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 dooskrzelowa lewostronna (Model/Catalog Number: 21-3245) is a medical device manufactured by SUMI spółka z ograniczoną odpowiedzialnością spółka komandytowa. This product is indexed under FDA Product Code / Category Classification R01040202 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 21-3245
Product Code / EMDN: R01040202
Device Name: Rurka dooskrzelowa lewostronna
Database Sync Date: 2026-08-09 16:29:13

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 dooskrzelowa lewostronna?

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

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05901292104795.

What classification code is assigned to this device?

This device is registered under product classification code R01040202.

Similar Classification Devices (R01040202)

Other Devices by SUMI spółka z ograniczoną odpowiedzialnością spółka komandytowa

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