Regenacyn Plus Scar Management Hydrogel (UDI 84875)
Manufactured by Sonoma Pharmaceuticals, Inc.
Device Regulatory Overview
The Regenacyn Plus Scar Management Hydrogel (Model/Catalog Number: 84875) is a medical device manufactured by Sonoma Pharmaceuticals, Inc.. This product is indexed under FDA Product Code / Category Classification PFP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 84875
- Product Code / EMDN
- PFP
- Device Name
- Database Sync Date
- 2026-08-09 10:03:32
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 Regenacyn Plus Scar Management Hydrogel?
The registered manufacturer of record for Regenacyn Plus Scar Management Hydrogel is Sonoma Pharmaceuticals, Inc..
What is the Primary UDI-DI identifier for Regenacyn Plus Scar Management Hydrogel?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 84875.
What classification code is assigned to this device?
This device is registered under product classification code PFP.
Similar Classification Devices (PFP)
Other Devices by Sonoma Pharmaceuticals, Inc.
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