eudamed_udi
Primary ID: 04260322415180
Arteo (UDI 04260322415180)
Manufactured by Andanza GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Arteo - Primary ID 04260322415180
Device Regulatory Overview
The Arteo (Model/Catalog Number: HIPL1050) is a medical device manufactured by Andanza GmbH. This product is indexed under FDA Product Code / Category Classification M030402010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HIPL1050
- Product Code / EMDN
- M030402010101
- Device Name
- Arteo Hip Spica o.S. Gr. 5
- Database Sync Date
- 2026-08-09 16:50:53
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 Arteo?
The registered manufacturer of record for Arteo is Andanza GmbH.
What is the Primary UDI-DI identifier for Arteo?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260322415180.
What classification code is assigned to this device?
This device is registered under product classification code M030402010101.
Similar Classification Devices (M030402010101)
Other Devices by Andanza GmbH
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