gudid
Primary ID: 795268
Philips FetView (UDI 795268)
Manufactured by Philips Ultrasound LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Philips FetView - Primary ID 795268
Device Regulatory Overview
The Philips FetView (Model/Catalog Number: 795268) is a medical device manufactured by Philips Ultrasound LLC. This product is indexed under FDA Product Code / Category Classification LMD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 795268
- Product Code / EMDN
- LMD
- Device Name
- Submission for Philips FetView version 1.10.0 Initial release
- 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 Philips FetView?
The registered manufacturer of record for Philips FetView is Philips Ultrasound LLC.
What is the Primary UDI-DI identifier for Philips FetView?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 795268.
What classification code is assigned to this device?
This device is registered under product classification code LMD.
Similar Classification Devices (LMD)
Other Devices by Philips Ultrasound LLC
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