gudid
Primary ID: 795007
Lumify Diagnostic Ultrasound System (UDI 795007)
Manufactured by Philips Ultrasound LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Lumify Diagnostic Ultrasound System - Primary ID 795007
Device Regulatory Overview
The Lumify Diagnostic Ultrasound System (Model/Catalog Number: 795007) is a medical device manufactured by Philips Ultrasound LLC. This product is indexed under FDA Product Code / Category Classification ITX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 795007
- Product Code / EMDN
- ITX
- Device Name
- Lumify Rugged System Bundle
- Database Sync Date
- 2026-08-09 09:45:39
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 Lumify Diagnostic Ultrasound System?
The registered manufacturer of record for Lumify Diagnostic Ultrasound System is Philips Ultrasound LLC.
What is the Primary UDI-DI identifier for Lumify Diagnostic Ultrasound System?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 795007.
What classification code is assigned to this device?
This device is registered under product classification code ITX.
Similar Classification Devices (ITX)
Other Devices by Philips Ultrasound LLC
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