eudamed_udi
Primary ID: 00854763005549
Epifoam (UDI 00854763005549)
Manufactured by BIODERMIS LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Epifoam - Primary ID 00854763005549
Device Regulatory Overview
The Epifoam (Model/Catalog Number: EPFU-W6) is a medical device manufactured by BIODERMIS LLC. This product is indexed under FDA Product Code / Category Classification M040299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- EPFU-W6
- Product Code / EMDN
- M040299
- Device Name
- Compression Foam
- Database Sync Date
- 2026-08-09 16:29:00
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 Epifoam?
The registered manufacturer of record for Epifoam is BIODERMIS LLC.
What is the Primary UDI-DI identifier for Epifoam?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00854763005549.
What classification code is assigned to this device?
This device is registered under product classification code M040299.
Similar Classification Devices (M040299)
Other Devices by BIODERMIS LLC
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