gudid
Primary ID: 1G
Preempt Plus RTU (US) (UDI 1G)
Manufactured by Virox Technologies Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Preempt Plus RTU (US) - Primary ID 1G
Device Regulatory Overview
The Preempt Plus RTU (US) (Model/Catalog Number: 1G) is a medical device manufactured by Virox Technologies Inc. This product is indexed under FDA Product Code / Category Classification LRJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1G
- Product Code / EMDN
- LRJ
- Device Name
- Database Sync Date
- 2026-08-09 09:08:48
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 Preempt Plus RTU (US)?
The registered manufacturer of record for Preempt Plus RTU (US) is Virox Technologies Inc.
What is the Primary UDI-DI identifier for Preempt Plus RTU (US)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1G.
What classification code is assigned to this device?
This device is registered under product classification code LRJ.
Similar Classification Devices (LRJ)
Other Devices by Virox Technologies Inc
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