gudid
Primary ID: BR900-2314
BR Surgical, LLC (UDI BR900-2314)
Manufactured by BR Surgical, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BR Surgical, LLC - Primary ID BR900-2314
Device Regulatory Overview
The BR Surgical, LLC (Model/Catalog Number: BR900-2314) is a medical device manufactured by BR Surgical, LLC. This product is indexed under FDA Product Code / Category Classification NTN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BR900-2314
- Product Code / EMDN
- NTN
- Device Name
- BR LED 300 watt Light Source, automatic light sensor, with Storz port
- Database Sync Date
- 2026-08-09 09:49:27
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 BR Surgical, LLC?
The registered manufacturer of record for BR Surgical, LLC is BR Surgical, LLC.
What is the Primary UDI-DI identifier for BR Surgical, LLC?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BR900-2314.
What classification code is assigned to this device?
This device is registered under product classification code NTN.
Similar Classification Devices (NTN)
Other Devices by BR Surgical, LLC
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