gudid
Primary ID: 038-990-102U
ProVu (UDI 038-990-102U)
Manufactured by FLEXICARE MEDICAL LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ProVu - Primary ID 038-990-102U
Device Regulatory Overview
The ProVu (Model/Catalog Number: 038-990-102U) is a medical device manufactured by FLEXICARE MEDICAL LIMITED. This product is indexed under FDA Product Code / Category Classification FOX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 038-990-102U
- Product Code / EMDN
- FOX
- Device Name
- ProVu Display Table Stand
- Database Sync Date
- 2026-08-09 09:08:16
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 ProVu?
The registered manufacturer of record for ProVu is FLEXICARE MEDICAL LIMITED.
What is the Primary UDI-DI identifier for ProVu?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 038-990-102U.
What classification code is assigned to this device?
This device is registered under product classification code FOX.
Similar Classification Devices (FOX)
Other Devices by FLEXICARE MEDICAL LIMITED
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