gudid
Primary ID: NAY3
Senographe Pristina (UDI NAY3)
Manufactured by GE MEDICAL SYSTEMS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Senographe Pristina - Primary ID NAY3
Device Regulatory Overview
The Senographe Pristina (Model/Catalog Number: NAY3) is a medical device manufactured by GE MEDICAL SYSTEMS. This product is indexed under FDA Product Code / Category Classification MUE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NAY3
- Product Code / EMDN
- MUE
- Device Name
- Senographe Pristina 3D UDI
- Database Sync Date
- 2026-08-09 09:14:30
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 Senographe Pristina?
The registered manufacturer of record for Senographe Pristina is GE MEDICAL SYSTEMS.
What is the Primary UDI-DI identifier for Senographe Pristina?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is NAY3.
What classification code is assigned to this device?
This device is registered under product classification code MUE.
Similar Classification Devices (MUE)
Other Devices by GE MEDICAL SYSTEMS
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