gudid Primary ID: UNITY 2 CONTROL UNIT WITHOUT CALIBRATION

Siemens (UDI UNITY 2 CONTROL UNIT WITHOUT CALIBRATION)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Siemens (Model/Catalog Number: UNITY 2 CONTROL UNIT WITHOUT CALIBRATION) is a medical device manufactured by Ws Audiology Usa, Inc.. This product is indexed under FDA Product Code / Category Classification EWO within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: UNITY 2 CONTROL UNIT WITHOUT CALIBRATION
Product Code / EMDN: EWO
Device Name: Siemens UNITY 2 CONTROL UNIT WITHOUT CALIBRATION
Database Sync Date: 2026-08-09 09:10:21

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 Siemens?

The registered manufacturer of record for Siemens is Ws Audiology Usa, Inc..

What is the Primary UDI-DI identifier for Siemens?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is UNITY 2 CONTROL UNIT WITHOUT CALIBRATION.

What classification code is assigned to this device?

This device is registered under product classification code EWO.

Similar Classification Devices (EWO)

Other Devices by Ws Audiology Usa, Inc.

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