eudamed_udi
Primary ID: 04751042630019
Magnetite (UDI 04751042630019)
Manufactured by SIA Laboveritas
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Magnetite - Primary ID 04751042630019
Device Regulatory Overview
The Magnetite (Model/Catalog Number: 070102) is a medical device manufactured by SIA Laboveritas. This product is indexed under FDA Product Code / Category Classification W0299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 070102
- Product Code / EMDN
- W0299
- Device Name
- Automate NA exctractor, with preinstalled software on board.
- Database Sync Date
- 2026-08-09 16:45:07
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 Magnetite?
The registered manufacturer of record for Magnetite is SIA Laboveritas.
What is the Primary UDI-DI identifier for Magnetite?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04751042630019.
What classification code is assigned to this device?
This device is registered under product classification code W0299.
Similar Classification Devices (W0299)
Other Devices by SIA Laboveritas
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