gudid
Primary ID: 10395
CUBE 30 touch (UDI 10395)
Manufactured by DIESSE DIAGNOSTICA SENESE SPA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CUBE 30 touch - Primary ID 10395
Device Regulatory Overview
The CUBE 30 touch (Model/Catalog Number: 10395) 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
- 10395
- 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 CUBE 30 touch?
The registered manufacturer of record for CUBE 30 touch is DIESSE DIAGNOSTICA SENESE SPA.
What is the Primary UDI-DI identifier for CUBE 30 touch?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10395.
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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