gudid
Primary ID: 9500-0000-0000
LED Daylite REVEAL (UDI 9500-0000-0000)
Manufactured by Designs For Vision, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LED Daylite REVEAL - Primary ID 9500-0000-0000
Device Regulatory Overview
The LED Daylite REVEAL (Model/Catalog Number: 9500-0000-0000) is a medical device manufactured by Designs For Vision, Inc.. This product is indexed under FDA Product Code / Category Classification QCR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9500-0000-0000
- Product Code / EMDN
- QCR
- Device Name
- The REVEAL FC is indicated for use as a wound autofluorescence imaging device to view autofluorescence images from skin wounds that are exposed to its excitation light.
- Database Sync Date
- 2026-08-09 09:09:55
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 LED Daylite REVEAL?
The registered manufacturer of record for LED Daylite REVEAL is Designs For Vision, Inc..
What is the Primary UDI-DI identifier for LED Daylite REVEAL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 9500-0000-0000.
What classification code is assigned to this device?
This device is registered under product classification code QCR.
Similar Classification Devices (QCR)
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