GUDIDData
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eudamed_udi Primary ID: 00850040133059

DR. BRACE ELITE Knee Brace with Side Stabilizers & Patella Gel Pads (Orion's XL) (UDI 00850040133059)

Manufactured by Dr. Brace LLC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DR. BRACE ELITE Knee Brace with Side Stabilizers & Patella Gel Pads (Orion's XL) - Primary ID 00850040133059

Device Regulatory Overview

The DR. BRACE ELITE Knee Brace with Side Stabilizers & Patella Gel Pads (Orion's XL) (Model/Catalog Number: CJ-LQP0-JMDX-EU) is a medical device manufactured by Dr. Brace LLC. This product is indexed under FDA Product Code / Category Classification M030501 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
CJ-LQP0-JMDX-EU
Product Code / EMDN
M030501
Device Name
DR. BRACE ELITE Knee Brace with Side Stabilizers & Patella Gel Pads
Database Sync Date
2026-08-09 16:29:45

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 DR. BRACE ELITE Knee Brace with Side Stabilizers & Patella Gel Pads (Orion's XL)?

The registered manufacturer of record for DR. BRACE ELITE Knee Brace with Side Stabilizers & Patella Gel Pads (Orion's XL) is Dr. Brace LLC.

What is the Primary UDI-DI identifier for DR. BRACE ELITE Knee Brace with Side Stabilizers & Patella Gel Pads (Orion's XL)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00850040133059.

What classification code is assigned to this device?

This device is registered under product classification code M030501.

Similar Classification Devices (M030501)

Other Devices by Dr. Brace LLC

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