eudamed_udi
Primary ID: 04251143403241
4-motion® Tibiabohrer (UDI 04251143403241)
Manufactured by ARTIQO GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 4-motion® Tibiabohrer - Primary ID 04251143403241
Device Regulatory Overview
The 4-motion® Tibiabohrer (Model/Catalog Number: 9210502) is a medical device manufactured by ARTIQO GmbH. This product is indexed under FDA Product Code / Category Classification L091102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9210502
- Product Code / EMDN
- L091102
- Device Name
- Klasse IIa Instrumente, chirurgisch invasiv, wiederverwendbar; maschinell angetriebene Instrumente, Bohrer
- Database Sync Date
- 2026-08-09 16:30:27
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® Tibiabohrer?
The registered manufacturer of record for 4-motion® Tibiabohrer is ARTIQO GmbH.
What is the Primary UDI-DI identifier for 4-motion® Tibiabohrer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251143403241.
What classification code is assigned to this device?
This device is registered under product classification code L091102.
Similar Classification Devices (L091102)
Other Devices by ARTIQO GmbH
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