gudid Primary ID: 93852

Uni-Wedge Regular ( Orange) (UDI 93852)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Uni-Wedge Regular ( Orange) (Model/Catalog Number: 93852) is a medical device manufactured by HAGER WORLDWIDE, INC.. This product is indexed under FDA Product Code / Category Classification EIF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 93852
Product Code / EMDN: EIF
Device Name: Dental wedges
Database Sync Date: 2026-08-09 09:03:09

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 Uni-Wedge Regular ( Orange)?

The registered manufacturer of record for Uni-Wedge Regular ( Orange) is HAGER WORLDWIDE, INC..

What is the Primary UDI-DI identifier for Uni-Wedge Regular ( Orange)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 93852.

What classification code is assigned to this device?

This device is registered under product classification code EIF.

Similar Classification Devices (EIF)

Other Devices by HAGER WORLDWIDE, INC.

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