gudid Primary ID: 118214

Astek (UDI 118214)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Astek (Model/Catalog Number: 118214) is a medical device manufactured by Young Innovations, Inc.. This product is indexed under FDA Product Code / Category Classification EHY within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 118214
Product Code / EMDN: EHY
Device Name: Transform Tray - Dentate - Mixed Bag 2 x #1-6
Database Sync Date: 2026-08-09 09:08:08

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 Astek?

The registered manufacturer of record for Astek is Young Innovations, Inc..

What is the Primary UDI-DI identifier for Astek?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 118214.

What classification code is assigned to this device?

This device is registered under product classification code EHY.

Similar Classification Devices (EHY)

Other Devices by Young Innovations, Inc.

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