gudid
Primary ID: UNITY 2 TEST BOX
Siemens (UDI UNITY 2 TEST BOX)
Manufactured by Ws Audiology Usa, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Siemens - Primary ID UNITY 2 TEST BOX
Device Regulatory Overview
The Siemens (Model/Catalog Number: UNITY 2 TEST BOX) 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 TEST BOX
- Product Code / EMDN
- EWO
- Device Name
- Siemens UNITY 2 TEST BOX
- 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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Get API Token Access ($49/mo)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 TEST BOX.
What classification code is assigned to this device?
This device is registered under product classification code EWO.
Similar Classification Devices (EWO)
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