gudid
Primary ID: 86040
Advanced Scar & Wound Hydrogel (UDI 86040)
Manufactured by Sonoma Pharmaceuticals, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Advanced Scar & Wound Hydrogel - Primary ID 86040
Device Regulatory Overview
The Advanced Scar & Wound Hydrogel (Model/Catalog Number: 86040) 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
- 86040
- Product Code / EMDN
- PFP
- Device Name
- Database Sync Date
- 2026-08-09 09:18:29
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 Advanced Scar & Wound Hydrogel?
The registered manufacturer of record for Advanced Scar & Wound Hydrogel is Sonoma Pharmaceuticals, Inc..
What is the Primary UDI-DI identifier for Advanced Scar & Wound Hydrogel?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 86040.
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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