eudamed_udi
Primary ID: 00852260000838
Dermasof (UDI 00852260000838)
Manufactured by BIODERMIS LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Dermasof - Primary ID 00852260000838
Device Regulatory Overview
The Dermasof (Model/Catalog Number: DMP-1) 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
- DMP-1
- Product Code / EMDN
- M04040701
- Device Name
- Silicone Gel Sheeting
- Database Sync Date
- 2026-08-09 16:30:12
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 Dermasof?
The registered manufacturer of record for Dermasof is BIODERMIS LLC.
What is the Primary UDI-DI identifier for Dermasof?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00852260000838.
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
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