gudid
Primary ID: DSF
Destiny System Fluid (UDI DSF)
Manufactured by TCOAG IRELAND LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Destiny System Fluid - Primary ID DSF
Device Regulatory Overview
The Destiny System Fluid (Model/Catalog Number: DSF) is a medical device manufactured by TCOAG IRELAND LIMITED. This product is indexed under FDA Product Code / Category Classification JPA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DSF
- Product Code / EMDN
- JPA
- Device Name
- Database Sync Date
- 2026-08-09 09:22:50
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 Destiny System Fluid?
The registered manufacturer of record for Destiny System Fluid is TCOAG IRELAND LIMITED.
What is the Primary UDI-DI identifier for Destiny System Fluid?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DSF.
What classification code is assigned to this device?
This device is registered under product classification code JPA.
Similar Classification Devices (JPA)
Other Devices by TCOAG IRELAND LIMITED
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