gudid
Primary ID: SpiroWay
SpiroWay (UDI SpiroWay)
Manufactured by eResearchTechnology GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SpiroWay - Primary ID SpiroWay
Device Regulatory Overview
The SpiroWay (Model/Catalog Number: SpiroWay) is a medical device manufactured by eResearchTechnology GmbH. This product is indexed under FDA Product Code / Category Classification BZG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SpiroWay
- Product Code / EMDN
- BZG
- Device Name
- Mouthpiece, accessory to spirometer
- Database Sync Date
- 2026-08-09 09:26:03
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 SpiroWay?
The registered manufacturer of record for SpiroWay is eResearchTechnology GmbH.
What is the Primary UDI-DI identifier for SpiroWay?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SpiroWay.
What classification code is assigned to this device?
This device is registered under product classification code BZG.
Similar Classification Devices (BZG)
Other Devices by eResearchTechnology GmbH
Programmatic Export
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JSON API Endpoint