gudid
Primary ID: V-892900
Vyaire (UDI V-892900)
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 V-892900
Device Regulatory Overview
The Vyaire (Model/Catalog Number: V-892900) is a medical device manufactured by Jaeger Medical GmbH. This product is indexed under FDA Product Code / Category Classification BXJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- V-892900
- Product Code / EMDN
- BXJ
- Device Name
- Nose clip
- Database Sync Date
- 2026-08-09 09:29:20
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
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 V-892900.
What classification code is assigned to this device?
This device is registered under product classification code BXJ.
Similar Classification Devices (BXJ)
Other Devices by Jaeger Medical GmbH
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint