eudamed_udi
Primary ID: 04251143403784
4-motion® Verlängerung für Ausrichtstab (UDI 04251143403784)
Manufactured by ARTIQO GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 4-motion® Verlängerung für Ausrichtstab - Primary ID 04251143403784
Device Regulatory Overview
The 4-motion® Verlängerung für Ausrichtstab (Model/Catalog Number: 9211512) is a medical device manufactured by ARTIQO GmbH. This product is indexed under FDA Product Code / Category Classification L091199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9211512
- Product Code / EMDN
- L091199
- Device Name
- Klasse Ir Instrumente, allgemeine chirurgisch invasive des 4-motion® Kniesystems, wiederverwendbar; sonstige wiederverwendbare invasive Instrumente
- Database Sync Date
- 2026-08-09 16:29:03
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® Verlängerung für Ausrichtstab?
The registered manufacturer of record for 4-motion® Verlängerung für Ausrichtstab is ARTIQO GmbH.
What is the Primary UDI-DI identifier for 4-motion® Verlängerung für Ausrichtstab?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251143403784.
What classification code is assigned to this device?
This device is registered under product classification code L091199.
Similar Classification Devices (L091199)
Other Devices by ARTIQO GmbH
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