eudamed_udi
Primary ID: 10603295476337
ATTUNE KNEE SYSTEM (UDI 10603295476337)
Manufactured by DePuy Ireland UC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ATTUNE KNEE SYSTEM - Primary ID 10603295476337
Device Regulatory Overview
The ATTUNE KNEE SYSTEM (Model/Catalog Number: 2549-00-250) is a medical device manufactured by DePuy Ireland UC. This product is indexed under FDA Product Code / Category Classification L0999 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2549-00-250
- Product Code / EMDN
- L0999
- Device Name
- Instrument Case/Tray
- Database Sync Date
- 2026-08-09 16:28:50
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 ATTUNE KNEE SYSTEM?
The registered manufacturer of record for ATTUNE KNEE SYSTEM is DePuy Ireland UC.
What is the Primary UDI-DI identifier for ATTUNE KNEE SYSTEM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10603295476337.
What classification code is assigned to this device?
This device is registered under product classification code L0999.
Similar Classification Devices (L0999)
Other Devices by DePuy Ireland UC
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