gudid
Primary ID: 875230
Midwest E Plus (UDI 875230)
Manufactured by SIRONA Dental Systems GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Midwest E Plus - Primary ID 875230
Device Regulatory Overview
The Midwest E Plus (Model/Catalog Number: 875230) is a medical device manufactured by SIRONA Dental Systems GmbH. This product is indexed under FDA Product Code / Category Classification EFB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 875230
- Product Code / EMDN
- EFB
- Device Name
- Midwest E Plus 1:1 S
- Database Sync Date
- 2026-08-09 09:07:31
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 Midwest E Plus?
The registered manufacturer of record for Midwest E Plus is SIRONA Dental Systems GmbH.
What is the Primary UDI-DI identifier for Midwest E Plus?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 875230.
What classification code is assigned to this device?
This device is registered under product classification code EFB.
Similar Classification Devices (EFB)
Other Devices by SIRONA Dental Systems GmbH
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