gudid
Primary ID: 795202
EPIQ 7 DIAGNOSTIC ULTRASOUND SYSTEM (UDI 795202)
Manufactured by Philips Ultrasound LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EPIQ 7 DIAGNOSTIC ULTRASOUND SYSTEM - Primary ID 795202
Device Regulatory Overview
The EPIQ 7 DIAGNOSTIC ULTRASOUND SYSTEM (Model/Catalog Number: 795202) is a medical device manufactured by Philips Ultrasound LLC. This product is indexed under FDA Product Code / Category Classification QIH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 795202
- Product Code / EMDN
- QIH
- Device Name
- Software version - 10.0.x
- 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 EPIQ 7 DIAGNOSTIC ULTRASOUND SYSTEM?
The registered manufacturer of record for EPIQ 7 DIAGNOSTIC ULTRASOUND SYSTEM is Philips Ultrasound LLC.
What is the Primary UDI-DI identifier for EPIQ 7 DIAGNOSTIC ULTRASOUND SYSTEM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 795202.
What classification code is assigned to this device?
This device is registered under product classification code QIH.
Similar Classification Devices (QIH)
Other Devices by Philips Ultrasound LLC
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