gudid
Primary ID: 93454
DermaFoam Heel/ Elbow Healogics by DermaRite (UDI 93454)
Manufactured by Sion Brands LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DermaFoam Heel/ Elbow Healogics by DermaRite - Primary ID 93454
Device Regulatory Overview
The DermaFoam Heel/ Elbow Healogics by DermaRite (Model/Catalog Number: 93454) 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
- 93454
- 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 Heel/ Elbow Healogics by DermaRite?
The registered manufacturer of record for DermaFoam Heel/ Elbow Healogics by DermaRite is Sion Brands LLC.
What is the Primary UDI-DI identifier for DermaFoam Heel/ Elbow Healogics by DermaRite?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 93454.
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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