gudid
Primary ID: RLH
Right Light (UDI RLH)
Manufactured by Xemax Surgical Products Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Right Light - Primary ID RLH
Device Regulatory Overview
The Right Light (Model/Catalog Number: RLH) is a medical device manufactured by Xemax Surgical Products Inc. This product is indexed under FDA Product Code / Category Classification KYT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RLH
- Product Code / EMDN
- KYT
- Device Name
- Battery powered head lamp.
- Database Sync Date
- 2026-08-09 09:03:36
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 Right Light?
The registered manufacturer of record for Right Light is Xemax Surgical Products Inc.
What is the Primary UDI-DI identifier for Right Light?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RLH.
What classification code is assigned to this device?
This device is registered under product classification code KYT.
Similar Classification Devices (KYT)
Other Devices by Xemax Surgical Products Inc
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