GUDIDData
eudamed_udi Primary ID: 04099637003221

Miratray 3 in 1, Full Arch 28er (UDI 04099637003221)

Manufactured by Hager & Werken GmbH & Co. KG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Miratray 3 in 1, Full Arch 28er - Primary ID 04099637003221

Device Regulatory Overview

The Miratray 3 in 1, Full Arch 28er (Model/Catalog Number: 101273) is a medical device manufactured by Hager & Werken GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification Q010503 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
101273
Product Code / EMDN
Q010503
Device Name
Abformlöffel, einmalige Anwendung
Database Sync Date
2026-08-09 16:30:33

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 Miratray 3 in 1, Full Arch 28er?

The registered manufacturer of record for Miratray 3 in 1, Full Arch 28er is Hager & Werken GmbH & Co. KG.

What is the Primary UDI-DI identifier for Miratray 3 in 1, Full Arch 28er?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04099637003221.

What classification code is assigned to this device?

This device is registered under product classification code Q010503.

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