eudamed_udi
Primary ID: 04048844600945
Actinia® (UDI 04048844600945)
Manufactured by implantcast GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Actinia® - Primary ID 04048844600945
Device Regulatory Overview
The Actinia® (Model/Catalog Number: 80049140) is a medical device manufactured by implantcast GmbH. This product is indexed under FDA Product Code / Category Classification L030199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 80049140
- Product Code / EMDN
- L030199
- Device Name
- -
- 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 Actinia®?
The registered manufacturer of record for Actinia® is implantcast GmbH.
What is the Primary UDI-DI identifier for Actinia®?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04048844600945.
What classification code is assigned to this device?
This device is registered under product classification code L030199.
Similar Classification Devices (L030199)
Other Devices by implantcast GmbH
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