gudid
Primary ID: WP20
Imex DOPPLER PROBE, 2MHZ, H2O PROOF PDII (UDI WP20)
Manufactured by IMEX, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Imex DOPPLER PROBE, 2MHZ, H2O PROOF PDII - Primary ID WP20
Device Regulatory Overview
The Imex DOPPLER PROBE, 2MHZ, H2O PROOF PDII (Model/Catalog Number: WP20) is a medical device manufactured by IMEX, LLC. This product is indexed under FDA Product Code / Category Classification KNG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- WP20
- Product Code / EMDN
- KNG
- Device Name
- Imex DOPPLER PROBE, 2MHZ, H2O PROOF PDII
- Database Sync Date
- 2026-08-09 09:37:38
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 Imex DOPPLER PROBE, 2MHZ, H2O PROOF PDII?
The registered manufacturer of record for Imex DOPPLER PROBE, 2MHZ, H2O PROOF PDII is IMEX, LLC.
What is the Primary UDI-DI identifier for Imex DOPPLER PROBE, 2MHZ, H2O PROOF PDII?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is WP20.
What classification code is assigned to this device?
This device is registered under product classification code KNG.
Similar Classification Devices (KNG)
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