gudid
Primary ID: RR190
Xguard (UDI RR190)
Manufactured by EMERSON & CO SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Xguard - Primary ID RR190
Device Regulatory Overview
The Xguard (Model/Catalog Number: RR190) is a medical device manufactured by EMERSON & CO SRL. This product is indexed under FDA Product Code / Category Classification LZC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RR190
- Product Code / EMDN
- LZC
- Device Name
- Radiation Reducing Glove
- Database Sync Date
- 2026-08-09 09:04:31
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 Xguard?
The registered manufacturer of record for Xguard is EMERSON & CO SRL.
What is the Primary UDI-DI identifier for Xguard?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RR190.
What classification code is assigned to this device?
This device is registered under product classification code LZC.
Similar Classification Devices (LZC)
Other Devices by EMERSON & CO SRL
Programmatic Export
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