gudid
Primary ID: A-LED5-99R
PeriOptix (UDI A-LED5-99R)
Manufactured by DEN-MAT HOLDINGS, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PeriOptix - Primary ID A-LED5-99R
Device Regulatory Overview
The PeriOptix (Model/Catalog Number: A-LED5-99R) 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
- A-LED5-99R
- Product Code / EMDN
- KYT
- Device Name
- Firefly Cordless Headlight System International Red
- 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 PeriOptix?
The registered manufacturer of record for PeriOptix is DEN-MAT HOLDINGS, LLC.
What is the Primary UDI-DI identifier for PeriOptix?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is A-LED5-99R.
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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