GUDIDData
gudid Primary ID: A-LED5-99B

PeriOptix (UDI A-LED5-99B)

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-LED5-99B

Device Regulatory Overview

The PeriOptix (Model/Catalog Number: A-LED5-99B) 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-LED5-99B
Product Code / EMDN
KYT
Device Name
Firefly Cordless Headlight system Internatinal Blue
Database Sync Date
2026-08-09 09:03:46

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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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-LED5-99B.

What classification code is assigned to this device?

This device is registered under product classification code KYT.

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