gudid
Primary ID: 942.655
NEOPLATE (UDI 942.655)
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 NEOPLATE - Primary ID 942.655
Device Regulatory Overview
The NEOPLATE (Model/Catalog Number: 942.655) is a medical device manufactured by Neoortho Produtos Ortopdicos S/A.. This product is indexed under FDA Product Code / Category Classification KWQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 942.655
- Product Code / EMDN
- KWQ
- Device Name
- Monocortical Cervical Screw SH D3.5x20 mm
- 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 NEOPLATE?
The registered manufacturer of record for NEOPLATE is Neoortho Produtos Ortopdicos S/A..
What is the Primary UDI-DI identifier for NEOPLATE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 942.655.
What classification code is assigned to this device?
This device is registered under product classification code KWQ.
Similar Classification Devices (KWQ)
Other Devices by Neoortho Produtos Ortopdicos S/A.
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