gudid Primary ID: B1073052

Universal (UDI B1073052)

Manufactured by Dentsply International Inc.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Universal (Model/Catalog Number: B1073052) is a medical device manufactured by Dentsply International Inc.. This product is indexed under FDA Product Code / Category Classification EGZ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: B1073052
Product Code / EMDN: EGZ
Device Name: UNIVRSL BITEWING HLDR ASSY KIT BLUE
Database Sync Date: 2026-08-09 09:02:02

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 Universal?

The registered manufacturer of record for Universal is Dentsply International Inc..

What is the Primary UDI-DI identifier for Universal?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is B1073052.

What classification code is assigned to this device?

This device is registered under product classification code EGZ.

Similar Classification Devices (EGZ)

Other Devices by Dentsply International Inc.

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