eudamed_udi
Primary ID: 04251143400257
4-motion® knee tibial component (UDI 04251143400257)
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 tibial component - Primary ID 04251143400257
Device Regulatory Overview
The 4-motion® knee tibial component (Model/Catalog Number: 4601-L005) is a medical device manufactured by ARTIQO GmbH. This product is indexed under FDA Product Code / Category Classification P090903020104 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4601-L005
- Product Code / EMDN
- P090903020104
- Device Name
- 4-motion® Tibia zementiert, links Gr. 5
- Database Sync Date
- 2026-08-09 16:30:08
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 tibial component?
The registered manufacturer of record for 4-motion® knee tibial component is ARTIQO GmbH.
What is the Primary UDI-DI identifier for 4-motion® knee tibial component?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251143400257.
What classification code is assigned to this device?
This device is registered under product classification code P090903020104.
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Other Devices by ARTIQO GmbH
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