eudamed_udi
Primary ID: 04251143400936
4-motion® knee patellar component (UDI 04251143400936)
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 patellar component - Primary ID 04251143400936
Device Regulatory Overview
The 4-motion® knee patellar component (Model/Catalog Number: 4101-0832) is a medical device manufactured by ARTIQO GmbH. This product is indexed under FDA Product Code / Category Classification P0909070201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4101-0832
- Product Code / EMDN
- P0909070201
- Device Name
- 4-motion® Patella zementiert,8 mm Ø32 mm
- Database Sync Date
- 2026-08-09 16:47:14
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 patellar component?
The registered manufacturer of record for 4-motion® knee patellar component is ARTIQO GmbH.
What is the Primary UDI-DI identifier for 4-motion® knee patellar component?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251143400936.
What classification code is assigned to this device?
This device is registered under product classification code P0909070201.
Similar Classification Devices (P0909070201)
Other Devices by ARTIQO GmbH
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