eudamed_udi
Primary ID: 07611819326446
LCP (UDI 07611819326446)
Manufactured by Synthes GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LCP - Primary ID 07611819326446
Device Regulatory Overview
The LCP (Model/Catalog Number: 68.120.109) is a medical device manufactured by Synthes GmbH. This product is indexed under FDA Product Code / Category Classification Z12011399 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 68.120.109
- Product Code / EMDN
- Z12011399
- Device Name
- Cases for Trauma/ CMF Devices
- Database Sync Date
- 2026-08-09 16:30:32
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 LCP?
The registered manufacturer of record for LCP is Synthes GmbH.
What is the Primary UDI-DI identifier for LCP?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07611819326446.
What classification code is assigned to this device?
This device is registered under product classification code Z12011399.
Similar Classification Devices (Z12011399)
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