gudid
Primary ID: UA2550-R
UbiqVue (UDI UA2550-R)
Manufactured by Lifesignals, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for UbiqVue - Primary ID UA2550-R
Device Regulatory Overview
The UbiqVue (Model/Catalog Number: UA2550-R) is a medical device manufactured by Lifesignals, Inc.. This product is indexed under FDA Product Code / Category Classification DRG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- UA2550-R
- Product Code / EMDN
- DRG
- Device Name
- Single Patient Relay Application
- Database Sync Date
- 2026-08-09 09:18:04
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 UbiqVue?
The registered manufacturer of record for UbiqVue is Lifesignals, Inc..
What is the Primary UDI-DI identifier for UbiqVue?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is UA2550-R.
What classification code is assigned to this device?
This device is registered under product classification code DRG.
Similar Classification Devices (DRG)
Other Devices by Lifesignals, Inc.
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