gudid
Primary ID: ES2824
Titan Touch (UDI ES2824)
Manufactured by Coloplast A/S
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Titan Touch - Primary ID ES2824
Device Regulatory Overview
The Titan Touch (Model/Catalog Number: ES2824) is a medical device manufactured by Coloplast A/S. This product is indexed under FDA Product Code / Category Classification FHW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ES2824
- Product Code / EMDN
- FHW
- Device Name
- Database Sync Date
- 2026-08-09 09:12:46
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 Titan Touch?
The registered manufacturer of record for Titan Touch is Coloplast A/S.
What is the Primary UDI-DI identifier for Titan Touch?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ES2824.
What classification code is assigned to this device?
This device is registered under product classification code FHW.
Similar Classification Devices (FHW)
Other Devices by Coloplast A/S
Programmatic Export
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JSON API Endpoint