eudamed_udi
Primary ID: 08053307591377
REVEAL MOBI-PRO 40kW (UDI 08053307591377)
Manufactured by Technix S.p.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for REVEAL MOBI-PRO 40kW - Primary ID 08053307591377
Device Regulatory Overview
The REVEAL MOBI-PRO 40kW (Model/Catalog Number: KAI-00022) is a medical device manufactured by Technix S.p.A.. This product is indexed under FDA Product Code / Category Classification Z11039016 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- KAI-00022
- Product Code / EMDN
- Z11039016
- Device Name
- Mobile radiologic units
- Database Sync Date
- 2026-08-09 16:30:24
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 REVEAL MOBI-PRO 40kW?
The registered manufacturer of record for REVEAL MOBI-PRO 40kW is Technix S.p.A..
What is the Primary UDI-DI identifier for REVEAL MOBI-PRO 40kW?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08053307591377.
What classification code is assigned to this device?
This device is registered under product classification code Z11039016.
Similar Classification Devices (Z11039016)
Other Devices by Technix S.p.A.
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