eudamed_udi Primary ID: 05907737310516

Jednorazowy ustnik do spirometru (UDI 05907737310516)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Jednorazowy ustnik do spirometru (Model/Catalog Number: PQUS-30) is a medical device manufactured by Pulmeq sp. z o.o.. This product is indexed under FDA Product Code / Category Classification Z12150185 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: PQUS-30
Product Code / EMDN: Z12150185
Device Name: Disposable spirometry mouthpiece
Database Sync Date: 2026-08-09 17:02:19

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 Jednorazowy ustnik do spirometru?

The registered manufacturer of record for Jednorazowy ustnik do spirometru is Pulmeq sp. z o.o..

What is the Primary UDI-DI identifier for Jednorazowy ustnik do spirometru?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05907737310516.

What classification code is assigned to this device?

This device is registered under product classification code Z12150185.

Similar Classification Devices (Z12150185)

Other Devices by Pulmeq sp. z o.o.

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