gudid
Primary ID: 93451
DermaFoam Healogics by DermaRite (UDI 93451)
Manufactured by Sion Brands LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DermaFoam Healogics by DermaRite - Primary ID 93451
Device Regulatory Overview
The DermaFoam Healogics by DermaRite (Model/Catalog Number: 93451) is a medical device manufactured by Sion Brands LLC. This product is indexed under FDA Product Code / Category Classification NAD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 93451
- Product Code / EMDN
- NAD
- Device Name
- Database Sync Date
- 2026-08-09 09:04:11
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 DermaFoam Healogics by DermaRite?
The registered manufacturer of record for DermaFoam Healogics by DermaRite is Sion Brands LLC.
What is the Primary UDI-DI identifier for DermaFoam Healogics by DermaRite?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 93451.
What classification code is assigned to this device?
This device is registered under product classification code NAD.
Similar Classification Devices (NAD)
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