eudamed_udi
Primary ID: 07611819354425
VA LCP (UDI 07611819354425)
Manufactured by Synthes GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VA LCP - Primary ID 07611819354425
Device Regulatory Overview
The VA LCP (Model/Catalog Number: 04.111.651S) is a medical device manufactured by Synthes GmbH. This product is indexed under FDA Product Code / Category Classification P09120501 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 04.111.651S
- Product Code / EMDN
- P09120501
- Device Name
- VA LCP Two-Column Volar Distal Radius Plate 2.4mm TiCP
- Database Sync Date
- 2026-08-09 16:28:44
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 VA LCP?
The registered manufacturer of record for VA LCP is Synthes GmbH.
What is the Primary UDI-DI identifier for VA LCP?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07611819354425.
What classification code is assigned to this device?
This device is registered under product classification code P09120501.
Similar Classification Devices (P09120501)
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