gudid
Primary ID: 922.405
NEOFACE (UDI 922.405)
Manufactured by Neoortho Produtos Ortopdicos S/A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NEOFACE - Primary ID 922.405
Device Regulatory Overview
The NEOFACE (Model/Catalog Number: 922.405) is a medical device manufactured by Neoortho Produtos Ortopdicos S/A.. This product is indexed under FDA Product Code / Category Classification JEY within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 922.405
- Product Code / EMDN
- JEY
- Device Name
- 6-Hole Locking Hard Miniplate
- Database Sync Date
- 2026-08-09 09:07:18
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 NEOFACE?
The registered manufacturer of record for NEOFACE is Neoortho Produtos Ortopdicos S/A..
What is the Primary UDI-DI identifier for NEOFACE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 922.405.
What classification code is assigned to this device?
This device is registered under product classification code JEY.
Similar Classification Devices (JEY)
Other Devices by Neoortho Produtos Ortopdicos S/A.
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