GUDIDData
gudid Primary ID: Q250290

Vivid PMMA Amann Girrbach System 12(H) A2 (UDI Q250290)

Manufactured by PEARSON DENTAL SUPPLIES, INC.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Vivid PMMA Amann Girrbach System 12(H) A2 - Primary ID Q250290

Device Regulatory Overview

The Vivid PMMA Amann Girrbach System 12(H) A2 (Model/Catalog Number: Q250290) is a medical device manufactured by PEARSON DENTAL SUPPLIES, INC.. This product is indexed under FDA Product Code / Category Classification ELL within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
Q250290
Product Code / EMDN
ELL
Device Name
25(H) A2
Database Sync Date
2026-08-09 09:15:03

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 Vivid PMMA Amann Girrbach System 12(H) A2?

The registered manufacturer of record for Vivid PMMA Amann Girrbach System 12(H) A2 is PEARSON DENTAL SUPPLIES, INC..

What is the Primary UDI-DI identifier for Vivid PMMA Amann Girrbach System 12(H) A2?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Q250290.

What classification code is assigned to this device?

This device is registered under product classification code ELL.

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