gudid
Primary ID: 795120
EPIQ 5 Ultrasound Circular Edition (UDI 795120)
Manufactured by Philips Ultrasound LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EPIQ 5 Ultrasound Circular Edition - Primary ID 795120
Device Regulatory Overview
The EPIQ 5 Ultrasound Circular Edition (Model/Catalog Number: 795120) is a medical device manufactured by Philips Ultrasound LLC. This product is indexed under FDA Product Code / Category Classification IYO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 795120
- Product Code / EMDN
- IYO
- Device Name
- Software Version 9.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 5 Ultrasound Circular Edition?
The registered manufacturer of record for EPIQ 5 Ultrasound Circular Edition is Philips Ultrasound LLC.
What is the Primary UDI-DI identifier for EPIQ 5 Ultrasound Circular Edition?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 795120.
What classification code is assigned to this device?
This device is registered under product classification code IYO.
Similar Classification Devices (IYO)
Other Devices by Philips Ultrasound LLC
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