gudid
Primary ID: CTY194-Unit-Plus-Uni-Pad
Brace Direct (UDI CTY194-Unit-Plus-Uni-Pad)
Manufactured by BRACE ALIGN LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Brace Direct - Primary ID CTY194-Unit-Plus-Uni-Pad
Device Regulatory Overview
The Brace Direct (Model/Catalog Number: CTY194-Unit-Plus-Uni-Pad) is a medical device manufactured by BRACE ALIGN LLC. This product is indexed under FDA Product Code / Category Classification ILO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CTY194-Unit-Plus-Uni-Pad
- Product Code / EMDN
- ILO
- Device Name
- Experience fast relief from muscle and joint pain with our state-of-the-art Frozen Ice Cold Therapy Machine. The ergonomic therapy pad provides comprehensive coverage, targeting areas like the knee, ankle, shoulder, and more, ensuring deep therapeutic comfort.
- Database Sync Date
- 2026-08-09 09:04:23
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 Brace Direct?
The registered manufacturer of record for Brace Direct is BRACE ALIGN LLC.
What is the Primary UDI-DI identifier for Brace Direct?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CTY194-Unit-Plus-Uni-Pad.
What classification code is assigned to this device?
This device is registered under product classification code ILO.
Similar Classification Devices (ILO)
Other Devices by BRACE ALIGN LLC
Programmatic Export
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