gudid
Primary ID: uDR 780i
uDR (UDI uDR 780i)
Manufactured by UIH TECHNOLOGIES LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for uDR - Primary ID uDR 780i
Device Regulatory Overview
The uDR (Model/Catalog Number: uDR 780i) is a medical device manufactured by UIH TECHNOLOGIES LLC. This product is indexed under FDA Product Code / Category Classification KPR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- uDR 780i
- Product Code / EMDN
- KPR
- Device Name
- The uDR 780i digital medical x-ray system is intended for use by a qualified/trained doctor or technician on both adult and pediatric subjects for taking diagnostic radiographic exposures of the skull, spinal column, chest, abdomen, extremities, and other anatomic sites. Applications can be performed with the subject sitting, standing, or lying in the prone or supine position. Not for mammography.
- Database Sync Date
- 2026-08-09 09:06:43
Full Regulatory Attributes
🔒 Token Gated
{
"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 uDR?
The registered manufacturer of record for uDR is UIH TECHNOLOGIES LLC.
What is the Primary UDI-DI identifier for uDR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is uDR 780i.
What classification code is assigned to this device?
This device is registered under product classification code KPR.
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