gudid
Primary ID: J722-5145
ORJ (UDI J722-5145)
Manufactured by Fortune Worldwide LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ORJ - Primary ID J722-5145
Device Regulatory Overview
The ORJ (Model/Catalog Number: J722-5145) is a medical device manufactured by Fortune Worldwide LLC. This product is indexed under FDA Product Code / Category Classification DZD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- J722-5145
- Product Code / EMDN
- DZD
- Device Name
- Orthodontic Metal Tubes for Teeth Correction
- Database Sync Date
- 2026-08-09 09:01:55
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 ORJ?
The registered manufacturer of record for ORJ is Fortune Worldwide LLC.
What is the Primary UDI-DI identifier for ORJ?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is J722-5145.
What classification code is assigned to this device?
This device is registered under product classification code DZD.
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