gudid Primary ID: 605211

Bite Block (UDI 605211)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Bite Block (Model/Catalog Number: 605211) 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: 605211
Product Code / EMDN: EIF
Device Name: Bite-Block Green (BX/4) 2/Large , 2/Small
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 Bite Block?

The registered manufacturer of record for Bite Block is HAGER WORLDWIDE, INC..

What is the Primary UDI-DI identifier for Bite Block?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 605211.

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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