NOMAD Pro 3 Packaged System, US (UDI 8.000.4875)
Manufactured by Dental Imaging Technologies Corporation
Device Regulatory Overview
The NOMAD Pro 3 Packaged System, US (Model/Catalog Number: 8.000.4875) is a medical device manufactured by Dental Imaging Technologies Corporation. This product is indexed under FDA Product Code / Category Classification EHD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 8.000.4875
- Product Code / EMDN
- EHD
- Device Name
- 2 batteries
- Database Sync Date
- 2026-08-09 09:01:55
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 NOMAD Pro 3 Packaged System, US?
The registered manufacturer of record for NOMAD Pro 3 Packaged System, US is Dental Imaging Technologies Corporation.
What is the Primary UDI-DI identifier for NOMAD Pro 3 Packaged System, US?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 8.000.4875.
What classification code is assigned to this device?
This device is registered under product classification code EHD.
Similar Classification Devices (EHD)
Other Devices by Dental Imaging Technologies Corporation
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