gudid
Primary ID: CR1074
Flashlite (UDI CR1074)
Manufactured by DEN-MAT HOLDINGS, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Flashlite - Primary ID CR1074
Device Regulatory Overview
The Flashlite (Model/Catalog Number: CR1074) is a medical device manufactured by DEN-MAT HOLDINGS, LLC. This product is indexed under FDA Product Code / Category Classification KYT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CR1074
- Product Code / EMDN
- KYT
- Device Name
- FL MAGNA POWER ADAPTER
- Database Sync Date
- 2026-08-09 09:03:46
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 Flashlite?
The registered manufacturer of record for Flashlite is DEN-MAT HOLDINGS, LLC.
What is the Primary UDI-DI identifier for Flashlite?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CR1074.
What classification code is assigned to this device?
This device is registered under product classification code KYT.
Similar Classification Devices (KYT)
Other Devices by DEN-MAT HOLDINGS, LLC
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