gudid
Primary ID: 709554
Vyaire (UDI 709554)
Manufactured by Jaeger Medical GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Vyaire - Primary ID 709554
Device Regulatory Overview
The Vyaire (Model/Catalog Number: 709554) is a medical device manufactured by Jaeger Medical GmbH. This product is indexed under FDA Product Code / Category Classification BTY within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 709554
- Product Code / EMDN
- BTY
- Device Name
- Pneumotach plastic PT 36, not heatable
- Database Sync Date
- 2026-08-09 09:29:20
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 Vyaire?
The registered manufacturer of record for Vyaire is Jaeger Medical GmbH.
What is the Primary UDI-DI identifier for Vyaire?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 709554.
What classification code is assigned to this device?
This device is registered under product classification code BTY.
Similar Classification Devices (BTY)
Other Devices by Jaeger Medical GmbH
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