gudid
Primary ID: FP1
TruCath (UDI FP1)
Manufactured by HR PHARMACEUTICALS INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TruCath - Primary ID FP1
Device Regulatory Overview
The TruCath (Model/Catalog Number: FP1) is a medical device manufactured by HR PHARMACEUTICALS INC.. This product is indexed under FDA Product Code / Category Classification OHR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FP1
- Product Code / EMDN
- OHR
- Device Name
- Foley Catheter Plug and Drain Tube Protector, Sterile
- Database Sync Date
- 2026-08-09 09:37:38
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 TruCath?
The registered manufacturer of record for TruCath is HR PHARMACEUTICALS INC..
What is the Primary UDI-DI identifier for TruCath?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FP1.
What classification code is assigned to this device?
This device is registered under product classification code OHR.
Similar Classification Devices (OHR)
Other Devices by HR PHARMACEUTICALS INC.
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