GUDIDData
gudid Primary ID: 93191

ComfortFoam Healogics by DermaRite (UDI 93191)

Manufactured by Sion Brands LLC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ComfortFoam Healogics by DermaRite - Primary ID 93191

Device Regulatory Overview

The ComfortFoam Healogics by DermaRite (Model/Catalog Number: 93191) 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
93191
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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Frequently Asked Questions

Who is the primary manufacturer of ComfortFoam Healogics by DermaRite?

The registered manufacturer of record for ComfortFoam Healogics by DermaRite is Sion Brands LLC.

What is the Primary UDI-DI identifier for ComfortFoam Healogics by DermaRite?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 93191.

What classification code is assigned to this device?

This device is registered under product classification code NAD.

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