GUDIDData
gudid Primary ID: V900

Velora RED (UDI V900)

Manufactured by Omm Imports Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Velora RED - Primary ID V900

Device Regulatory Overview

The Velora RED (Model/Catalog Number: V900) is a medical device manufactured by Omm Imports Inc.. This product is indexed under FDA Product Code / Category Classification OHS within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
V900
Product Code / EMDN
OHS
Device Name
Over the counter Red/infrared LED phototherapy lamp.
Database Sync Date
2026-08-09 09:37:50

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 Velora RED?

The registered manufacturer of record for Velora RED is Omm Imports Inc..

What is the Primary UDI-DI identifier for Velora RED?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is V900.

What classification code is assigned to this device?

This device is registered under product classification code OHS.

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