Prodia (UDI ASST-S)

Manufactured by ABRASIVE TECHNOLOGY, INC.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Prodia (Model/Catalog Number: ASST-S) is a medical device manufactured by ABRASIVE TECHNOLOGY, INC.. This product is indexed under FDA Product Code / Category Classification EHM within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: ASST-S
Product Code / EMDN: EHM
Device Name: Diamond Finishing Strips
Database Sync Date: 2026-08-09 09:06:21

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 Prodia?

The registered manufacturer of record for Prodia is ABRASIVE TECHNOLOGY, INC..

What is the Primary UDI-DI identifier for Prodia?

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

What classification code is assigned to this device?

This device is registered under product classification code EHM.

Similar Classification Devices (EHM)

Other Devices by ABRASIVE TECHNOLOGY, INC.

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