eudamed_udi
Primary ID: 10603295050537
Unspecified Brand (UDI 10603295050537)
Manufactured by DePuy Ireland UC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 10603295050537
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 1516-40-912) is a medical device manufactured by DePuy Ireland UC. This product is indexed under FDA Product Code / Category Classification P090903020202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1516-40-912
- Product Code / EMDN
- P090903020202
- Device Name
- Cemented FB Tibial Insert
- Database Sync Date
- 2026-08-09 16:29:35
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is DePuy Ireland UC.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10603295050537.
What classification code is assigned to this device?
This device is registered under product classification code P090903020202.
Similar Classification Devices (P090903020202)
Other Devices by DePuy Ireland UC
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