eudamed_udi
Primary ID: 04251143405283
4-motion® knee inlay (UDI 04251143405283)
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 inlay - Primary ID 04251143405283
Device Regulatory Overview
The 4-motion® knee inlay (Model/Catalog Number: 7411-0607) is a medical device manufactured by ARTIQO GmbH. This product is indexed under FDA Product Code / Category Classification P090903020202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 7411-0607
- Product Code / EMDN
- P090903020202
- Device Name
- 4-motion® Inlay VEX Gr. 6, 7 mm
- Database Sync Date
- 2026-08-09 16:30:22
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 inlay?
The registered manufacturer of record for 4-motion® knee inlay is ARTIQO GmbH.
What is the Primary UDI-DI identifier for 4-motion® knee inlay?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251143405283.
What classification code is assigned to this device?
This device is registered under product classification code P090903020202.
Similar Classification Devices (P090903020202)
Other Devices by ARTIQO GmbH
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