eudamed_udi
Primary ID: 04251143406181
Deckel für Sieb (UDI 04251143406181)
Manufactured by ARTIQO GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Deckel für Sieb - Primary ID 04251143406181
Device Regulatory Overview
The Deckel für Sieb (Model/Catalog Number: 9110001) is a medical device manufactured by ARTIQO GmbH. This product is indexed under FDA Product Code / Category Classification L0999 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9110001
- Product Code / EMDN
- L0999
- Device Name
- Klasse I Zubehör, nicht-invasive Instrumente des A2® Hüftschaftsystems, wiederverwendbar
- Database Sync Date
- 2026-08-09 16:48:49
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 Deckel für Sieb?
The registered manufacturer of record for Deckel für Sieb is ARTIQO GmbH.
What is the Primary UDI-DI identifier for Deckel für Sieb?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251143406181.
What classification code is assigned to this device?
This device is registered under product classification code L0999.
Similar Classification Devices (L0999)
Other Devices by ARTIQO GmbH
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