gudid
Primary ID: 3
Genesis Touch Application (UDI 3)
Manufactured by Mobilehelp, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Genesis Touch Application - Primary ID 3
Device Regulatory Overview
The Genesis Touch Application (Model/Catalog Number: 3) is a medical device manufactured by Mobilehelp, LLC. This product is indexed under FDA Product Code / Category Classification DRG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3
- Product Code / EMDN
- DRG
- Device Name
- Database Sync Date
- 2026-08-09 09:33:00
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 Genesis Touch Application?
The registered manufacturer of record for Genesis Touch Application is Mobilehelp, LLC.
What is the Primary UDI-DI identifier for Genesis Touch Application?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 3.
What classification code is assigned to this device?
This device is registered under product classification code DRG.
Similar Classification Devices (DRG)
Other Devices by Mobilehelp, LLC
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