PhytoLight (UDI PL1.0)

Manufactured by PhotoDynamic Incorporated

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The PhytoLight (Model/Catalog Number: PL1.0) is a medical device manufactured by PhotoDynamic Incorporated. This product is indexed under FDA Product Code / Category Classification EEG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: PL1.0
Product Code / EMDN: EEG
Device Name: Dental light device
Database Sync Date: 2026-08-09 09:32:43

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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Frequently Asked Questions

Who is the primary manufacturer of PhytoLight?

The registered manufacturer of record for PhytoLight is PhotoDynamic Incorporated.

What is the Primary UDI-DI identifier for PhytoLight?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PL1.0.

What classification code is assigned to this device?

This device is registered under product classification code EEG.

Similar Classification Devices (EEG)

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