eudamed_udi
Primary ID: 00852260000296
Pro-Sil (UDI 00852260000296)
Manufactured by BIODERMIS LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Pro-Sil - Primary ID 00852260000296
Device Regulatory Overview
The Pro-Sil (Model/Catalog Number: PROSP17-111) is a medical device manufactured by BIODERMIS LLC. This product is indexed under FDA Product Code / Category Classification M04040702 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PROSP17-111
- Product Code / EMDN
- M04040702
- Device Name
- Silicone Stick
- Database Sync Date
- 2026-08-09 16:50:44
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 Pro-Sil?
The registered manufacturer of record for Pro-Sil is BIODERMIS LLC.
What is the Primary UDI-DI identifier for Pro-Sil?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00852260000296.
What classification code is assigned to this device?
This device is registered under product classification code M04040702.
Similar Classification Devices (M04040702)
Other Devices by BIODERMIS LLC
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