gudid Primary ID: Long Medium

Diamond Wedge (UDI Long Medium)

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 Medium) 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 Medium
Product Code / EMDN: EJB
Device Name: Wedge used in dental restorations.
Database Sync Date: 2026-08-09 09:01:11

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

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 Medium.

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

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint