eudamed_udi
Primary ID: 00852260000074
Epiderm Natural (UDI 00852260000074)
Manufactured by BIODERMIS LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Epiderm Natural - Primary ID 00852260000074
Device Regulatory Overview
The Epiderm Natural (Model/Catalog Number: FPT-C51) is a medical device manufactured by BIODERMIS LLC. This product is indexed under FDA Product Code / Category Classification M04040701 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FPT-C51
- Product Code / EMDN
- M04040701
- Device Name
- Silicone Gel Sheeting
- Database Sync Date
- 2026-08-09 17:04:13
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Epiderm Natural?
The registered manufacturer of record for Epiderm Natural is BIODERMIS LLC.
What is the Primary UDI-DI identifier for Epiderm Natural?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00852260000074.
What classification code is assigned to this device?
This device is registered under product classification code M04040701.
Similar Classification Devices (M04040701)
Other Devices by BIODERMIS LLC
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint