gudid Primary ID: Ceramill Splintec 98x20 N/US

Ceramill Splintec (UDI Ceramill Splintec 98x20 N/US)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Ceramill Splintec (Model/Catalog Number: Ceramill Splintec 98x20 N/US) is a medical device manufactured by Merz Dental GmbH. This product is indexed under FDA Product Code / Category Classification MQC within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Ceramill Splintec 98x20 N/US
Product Code / EMDN: MQC
Device Name: Ceramill Splintec 98x20 N/US
Database Sync Date: 2026-08-09 09:02:54

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 Ceramill Splintec?

The registered manufacturer of record for Ceramill Splintec is Merz Dental GmbH.

What is the Primary UDI-DI identifier for Ceramill Splintec?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Ceramill Splintec 98x20 N/US.

What classification code is assigned to this device?

This device is registered under product classification code MQC.

Similar Classification Devices (MQC)

Other Devices by Merz Dental GmbH

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