eudamed_udi
Primary ID: 05059441131366
Tornado (UDI 05059441131366)
Manufactured by ArjoHuntleigh AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Tornado - Primary ID 05059441131366
Device Regulatory Overview
The Tornado (Model/Catalog Number: FA6N032130DPL0) is a medical device manufactured by ArjoHuntleigh AB. This product is indexed under FDA Product Code / Category Classification Z12011301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FA6N032130DPL0
- Product Code / EMDN
- Z12011301
- Device Name
- NINJO
- Database Sync Date
- 2026-08-09 16:28:54
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 Tornado?
The registered manufacturer of record for Tornado is ArjoHuntleigh AB.
What is the Primary UDI-DI identifier for Tornado?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05059441131366.
What classification code is assigned to this device?
This device is registered under product classification code Z12011301.
Similar Classification Devices (Z12011301)
Other Devices by ArjoHuntleigh AB
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