gudid
Primary ID: Titan Touch
Titan (UDI Titan Touch)
Manufactured by Coloplast A/S
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Titan - Primary ID Titan Touch
Device Regulatory Overview
The Titan (Model/Catalog Number: Titan Touch) 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
- Titan Touch
- Product Code / EMDN
- FHW
- Device Name
- Titan Touch Narrow Base Infrapubic Zero Angle 16cm
- Database Sync Date
- 2026-08-09 09:12:47
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?
The registered manufacturer of record for Titan is Coloplast A/S.
What is the Primary UDI-DI identifier for Titan?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Titan Touch.
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
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