gudid
Primary ID: 10392
MINI-CUBE (UDI 10392)
Manufactured by DIESSE DIAGNOSTICA SENESE SPA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MINI-CUBE - Primary ID 10392
Device Regulatory Overview
The MINI-CUBE (Model/Catalog Number: 10392) is a medical device manufactured by DIESSE DIAGNOSTICA SENESE SPA. This product is indexed under FDA Product Code / Category Classification GKB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10392
- Product Code / EMDN
- GKB
- Device Name
- Database Sync Date
- 2026-08-09 09:04:33
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 MINI-CUBE?
The registered manufacturer of record for MINI-CUBE is DIESSE DIAGNOSTICA SENESE SPA.
What is the Primary UDI-DI identifier for MINI-CUBE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10392.
What classification code is assigned to this device?
This device is registered under product classification code GKB.
Similar Classification Devices (GKB)
Other Devices by DIESSE DIAGNOSTICA SENESE SPA
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