gudid Primary ID: Long Extra Large

Diamond Wedge (UDI Long Extra Large)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Diamond Wedge (Model/Catalog Number: Long Extra Large) is a medical device manufactured by Bioclear Matrix Systems. This product is indexed under FDA Product Code / Category Classification EJB within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Long Extra Large
Product Code / EMDN: EJB
Device Name: Wedge used in dental restorations.
Database Sync Date: 2026-08-09 09:01:11

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 Diamond Wedge?

The registered manufacturer of record for Diamond Wedge is Bioclear Matrix Systems.

What is the Primary UDI-DI identifier for Diamond Wedge?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Long Extra Large.

What classification code is assigned to this device?

This device is registered under product classification code EJB.

Similar Classification Devices (EJB)

Other Devices by Bioclear Matrix Systems

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