eudamed_udi
Primary ID: 04251143406587
A2® short stem (UDI 04251143406587)
Manufactured by ARTIQO GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for A2® short stem - Primary ID 04251143406587
Device Regulatory Overview
The A2® short stem (Model/Catalog Number: 411308) is a medical device manufactured by ARTIQO GmbH. This product is indexed under FDA Product Code / Category Classification P090804010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 411308
- Product Code / EMDN
- P090804010101
- Device Name
- A2® Schaft Gr. 8 Typ B, zementiert
- Database Sync Date
- 2026-08-09 16:46:29
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 A2® short stem?
The registered manufacturer of record for A2® short stem is ARTIQO GmbH.
What is the Primary UDI-DI identifier for A2® short stem?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251143406587.
What classification code is assigned to this device?
This device is registered under product classification code P090804010101.
Similar Classification Devices (P090804010101)
Other Devices by ARTIQO GmbH
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