eudamed_udi Primary ID: 07350045121691

Test Lung 1000 ml (UDI 07350045121691)

Manufactured by Kanmed AB

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Test Lung 1000 ml (Model/Catalog Number: MY151022) is a medical device manufactured by Kanmed AB. This product is indexed under FDA Product Code / Category Classification R020199 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: MY151022
Product Code / EMDN: R020199
Device Name: Test Lung
Database Sync Date: 2026-08-09 16:48:09

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 Test Lung 1000 ml?

The registered manufacturer of record for Test Lung 1000 ml is Kanmed AB.

What is the Primary UDI-DI identifier for Test Lung 1000 ml?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07350045121691.

What classification code is assigned to this device?

This device is registered under product classification code R020199.

Similar Classification Devices (R020199)

Other Devices by Kanmed AB

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