eudamed_udi
Primary ID: 04251143401537
4-motion® knee femoral component (UDI 04251143401537)
Manufactured by ARTIQO GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 4-motion® knee femoral component - Primary ID 04251143401537
Device Regulatory Overview
The 4-motion® knee femoral component (Model/Catalog Number: 4811-LW08) is a medical device manufactured by ARTIQO GmbH. This product is indexed under FDA Product Code / Category Classification P0909030101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4811-LW08
- Product Code / EMDN
- P0909030101
- Device Name
- 4-motion® Femur zem. links Gr. 8w, TiNbN
- Database Sync Date
- 2026-08-09 16:29:06
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 4-motion® knee femoral component?
The registered manufacturer of record for 4-motion® knee femoral component is ARTIQO GmbH.
What is the Primary UDI-DI identifier for 4-motion® knee femoral component?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251143401537.
What classification code is assigned to this device?
This device is registered under product classification code P0909030101.
Similar Classification Devices (P0909030101)
Other Devices by ARTIQO GmbH
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