gudid
Primary ID: VP8XS-USA-DATA
DOPPLEX (UDI VP8XS-USA-DATA)
Manufactured by HUNTLEIGH HEALTHCARE LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DOPPLEX - Primary ID VP8XS-USA-DATA
Device Regulatory Overview
The DOPPLEX (Model/Catalog Number: VP8XS-USA-DATA) is a medical device manufactured by HUNTLEIGH HEALTHCARE LIMITED. This product is indexed under FDA Product Code / Category Classification JAF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- VP8XS-USA-DATA
- Product Code / EMDN
- JAF
- Device Name
- HIGH SENSITIVITY 8MHZ VASCULAR PROBE
- Database Sync Date
- 2026-08-09 09:39:57
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 DOPPLEX?
The registered manufacturer of record for DOPPLEX is HUNTLEIGH HEALTHCARE LIMITED.
What is the Primary UDI-DI identifier for DOPPLEX?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is VP8XS-USA-DATA.
What classification code is assigned to this device?
This device is registered under product classification code JAF.
Similar Classification Devices (JAF)
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