gudid Primary ID: GSI TympStar Pro

Grason-Stadler (UDI GSI TympStar Pro)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Grason-Stadler (Model/Catalog Number: GSI TympStar Pro) is a medical device manufactured by Diagnostic Group LLC. This product is indexed under FDA Product Code / Category Classification ETY within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: GSI TympStar Pro
Product Code / EMDN: ETY
Device Name
Database Sync Date: 2026-08-09 09:10:02

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 Grason-Stadler?

The registered manufacturer of record for Grason-Stadler is Diagnostic Group LLC.

What is the Primary UDI-DI identifier for Grason-Stadler?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is GSI TympStar Pro.

What classification code is assigned to this device?

This device is registered under product classification code ETY.

Similar Classification Devices (ETY)

Other Devices by Diagnostic Group LLC

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