gudid Primary ID: UM-3R-3

ULTRASONIC PROBE (UDI UM-3R-3)

Manufactured by OLYMPUS MEDICAL SYSTEMS CORP.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The ULTRASONIC PROBE (Model/Catalog Number: UM-3R-3) is a medical device manufactured by OLYMPUS MEDICAL SYSTEMS CORP.. This product is indexed under FDA Product Code / Category Classification ITX within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: UM-3R-3
Product Code / EMDN: ITX
Device Name
Database Sync Date: 2026-08-09 09:46:01

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 ULTRASONIC PROBE?

The registered manufacturer of record for ULTRASONIC PROBE is OLYMPUS MEDICAL SYSTEMS CORP..

What is the Primary UDI-DI identifier for ULTRASONIC PROBE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is UM-3R-3.

What classification code is assigned to this device?

This device is registered under product classification code ITX.

Similar Classification Devices (ITX)

Other Devices by OLYMPUS MEDICAL SYSTEMS CORP.

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