gudid
Primary ID: SD3 Vascular
Ultrasonic Pocket Doppler (UDI SD3 Vascular)
Manufactured by Edan Instruments, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ultrasonic Pocket Doppler - Primary ID SD3 Vascular
Device Regulatory Overview
The Ultrasonic Pocket Doppler (Model/Catalog Number: SD3 Vascular) is a medical device manufactured by Edan Instruments, Inc.. This product is indexed under FDA Product Code / Category Classification KNG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SD3 Vascular
- Product Code / EMDN
- KNG
- Device Name
- Database Sync Date
- 2026-08-09 09:11:06
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 Ultrasonic Pocket Doppler?
The registered manufacturer of record for Ultrasonic Pocket Doppler is Edan Instruments, Inc..
What is the Primary UDI-DI identifier for Ultrasonic Pocket Doppler?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SD3 Vascular.
What classification code is assigned to this device?
This device is registered under product classification code KNG.
Similar Classification Devices (KNG)
Other Devices by Edan Instruments, Inc.
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