gudid Primary ID: 605456

Spandex Vertical Lip Retractor (Adult) (UDI 605456)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Spandex Vertical Lip Retractor (Adult) (Model/Catalog Number: 605456) 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: 605456
Product Code / EMDN: EIF
Device Name: Dental Retractors
Database Sync Date: 2026-08-09 09:00:34

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 Spandex Vertical Lip Retractor (Adult)?

The registered manufacturer of record for Spandex Vertical Lip Retractor (Adult) is HAGER WORLDWIDE, INC..

What is the Primary UDI-DI identifier for Spandex Vertical Lip Retractor (Adult)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 605456.

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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