eudamed_udi
Primary ID: 05907737310530
Jednorazowy ustnik do spirometru (UDI 05907737310530)
Manufactured by Pulmeq sp. z o.o.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Jednorazowy ustnik do spirometru - Primary ID 05907737310530
Device Regulatory Overview
The Jednorazowy ustnik do spirometru (Model/Catalog Number: PQUS-22) 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-22
- Product Code / EMDN
- Z12150185
- Device Name
- Disposable spirometry mouthpiece
- Database Sync Date
- 2026-08-09 18:15:09
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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Get API Token Access ($49/mo)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 05907737310530.
What classification code is assigned to this device?
This device is registered under product classification code Z12150185.
Similar Classification Devices (Z12150185)
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