gudid
Primary ID: 90R0130
Radiance (UDI 90R0130)
Manufactured by Nds Surgical Imaging LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Radiance - Primary ID 90R0130
Device Regulatory Overview
The Radiance (Model/Catalog Number: 90R0130) is a medical device manufactured by Nds Surgical Imaging LLC. This product is indexed under FDA Product Code / Category Classification KQM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 90R0130
- Product Code / EMDN
- KQM
- Device Name
- RADIANCE ULTRA 32.0" 4K ZEROWIRE DUO, 12G SDI / 2D, SC-WK32-G1B27
- Database Sync Date
- 2026-08-09 09:32:54
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 Radiance?
The registered manufacturer of record for Radiance is Nds Surgical Imaging LLC.
What is the Primary UDI-DI identifier for Radiance?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 90R0130.
What classification code is assigned to this device?
This device is registered under product classification code KQM.
Similar Classification Devices (KQM)
Other Devices by Nds Surgical Imaging LLC
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