GUDIDData
gudid Primary ID: CTY243

Brace Direct (UDI CTY243)

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 CTY243

Device Regulatory Overview

The Brace Direct (Model/Catalog Number: CTY243) 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
CTY243
Product Code / EMDN
ILO
Device Name
Experience the next level of pain relief with the Brace Direct BlueIce Cold Cryotherapy Machine. Perfect for arthritis, post-surgical recovery, and injury treatment, this machine combines portability and efficiency for targeted cold therapy.
Database Sync Date
2026-08-09 09:04:21

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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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 CTY243.

What classification code is assigned to this device?

This device is registered under product classification code ILO.

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