gudid Primary ID: A19-0200

Vivid KoolWhite (UDI A19-0200)

Manufactured by PEARSON DENTAL SUPPLIES, INC.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Vivid KoolWhite (Model/Catalog Number: A19-0200) is a medical device manufactured by PEARSON DENTAL SUPPLIES, INC.. This product is indexed under FDA Product Code / Category Classification EEG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: A19-0200
Product Code / EMDN: EEG
Device Name
Database Sync Date: 2026-08-09 09:15:03

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 Vivid KoolWhite?

The registered manufacturer of record for Vivid KoolWhite is PEARSON DENTAL SUPPLIES, INC..

What is the Primary UDI-DI identifier for Vivid KoolWhite?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is A19-0200.

What classification code is assigned to this device?

This device is registered under product classification code EEG.

Similar Classification Devices (EEG)

Other Devices by PEARSON DENTAL SUPPLIES, INC.

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