eudamed_udi
Primary ID: 04251143400264
4-motion® knee tibial component (UDI 04251143400264)
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 04251143400264
Device Regulatory Overview
The 4-motion® knee tibial component (Model/Catalog Number: 4601-L006) 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-L006
- Product Code / EMDN
- P090903020104
- Device Name
- 4-motion® Tibia zementiert, links Gr. 6
- Database Sync Date
- 2026-08-09 16:46:37
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
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 04251143400264.
What classification code is assigned to this device?
This device is registered under product classification code P090903020104.
Similar Classification Devices (P090903020104)
Other Devices by ARTIQO GmbH
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint