gudid
Primary ID: 04.503.149S
MatrixNEURO (UDI 04.503.149S)
Manufactured by Synthes GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MatrixNEURO - Primary ID 04.503.149S
Device Regulatory Overview
The MatrixNEURO (Model/Catalog Number: 04.503.149S) is a medical device manufactured by Synthes GmbH. This product is indexed under FDA Product Code / Category Classification GXR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 04.503.149S
- Product Code / EMDN
- GXR
- Device Name
- TI MATRIXNEURO RECON MESH 70MM DIA/GOLD-STERILE
- Database Sync Date
- 2026-08-09 09:39:08
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 MatrixNEURO?
The registered manufacturer of record for MatrixNEURO is Synthes GmbH.
What is the Primary UDI-DI identifier for MatrixNEURO?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04.503.149S.
What classification code is assigned to this device?
This device is registered under product classification code GXR.
Similar Classification Devices (GXR)
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