gudid Primary ID: 1242

Meron (UDI 1242)

Manufactured by VOCO GmbH

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Meron (Model/Catalog Number: 1242) is a medical device manufactured by VOCO GmbH. This product is indexed under FDA Product Code / Category Classification EMA within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 1242
Product Code / EMDN: EMA
Device Name: Dual-curing universal composite-based luting system.For all materials (metal, composite inlays and ceramic, also zirconium dioxide).Bubble-free perfect mixing.Direct application.Excellent adhesion to dentine, enamel and to metals.Special one-step Ceramic bond for optimal adhesion to porcelain.Radiopaque.Available in three shadese.Try-In pastes simplify shade selection before cementation.All-in-one set.
Database Sync Date: 2026-08-09 09:07:36

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 Meron?

The registered manufacturer of record for Meron is VOCO GmbH.

What is the Primary UDI-DI identifier for Meron?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1242.

What classification code is assigned to this device?

This device is registered under product classification code EMA.

Similar Classification Devices (EMA)

Other Devices by VOCO GmbH

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