gudid
Primary ID: EWP2040
Wittmann Patch (UDI EWP2040)
Manufactured by PRESERVATION SOLUTIONS INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Wittmann Patch - Primary ID EWP2040
Device Regulatory Overview
The Wittmann Patch (Model/Catalog Number: EWP2040) is a medical device manufactured by PRESERVATION SOLUTIONS INC. This product is indexed under FDA Product Code / Category Classification FTL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- EWP2040
- Product Code / EMDN
- FTL
- Device Name
- For temporary bridging of abdominal wall openings where primary closure is not possible and/or repeat abdominal entries are necessary.
- Database Sync Date
- 2026-08-09 09:22:17
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 Wittmann Patch?
The registered manufacturer of record for Wittmann Patch is PRESERVATION SOLUTIONS INC.
What is the Primary UDI-DI identifier for Wittmann Patch?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is EWP2040.
What classification code is assigned to this device?
This device is registered under product classification code FTL.
Similar Classification Devices (FTL)
Other Devices by PRESERVATION SOLUTIONS INC
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