gudid
Primary ID: 930.252
NEONAIL (UDI 930.252)
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 NEONAIL - Primary ID 930.252
Device Regulatory Overview
The NEONAIL (Model/Catalog Number: 930.252) is a medical device manufactured by Neoortho Produtos Ortopdicos S/A.. This product is indexed under FDA Product Code / Category Classification FZX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 930.252
- Product Code / EMDN
- FZX
- Device Name
- Intramedullary Nail Extractor
- Database Sync Date
- 2026-08-09 09:07:11
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 NEONAIL?
The registered manufacturer of record for NEONAIL is Neoortho Produtos Ortopdicos S/A..
What is the Primary UDI-DI identifier for NEONAIL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 930.252.
What classification code is assigned to this device?
This device is registered under product classification code FZX.
Similar Classification Devices (FZX)
Other Devices by Neoortho Produtos Ortopdicos S/A.
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