gudid
Primary ID: A
PowerCube+ Series (UDI A)
Manufactured by Ganshorn Medizin Electronic GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PowerCube+ Series - Primary ID A
Device Regulatory Overview
The PowerCube+ Series (Model/Catalog Number: A) is a medical device manufactured by Ganshorn Medizin Electronic GmbH. This product is indexed under FDA Product Code / Category Classification JEH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- A
- Product Code / EMDN
- JEH
- Device Name
- The PowerCube Diffusion+ is equipped with the MultiX Trolley.
- Database Sync Date
- 2026-08-09 09:44:46
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 PowerCube+ Series?
The registered manufacturer of record for PowerCube+ Series is Ganshorn Medizin Electronic GmbH.
What is the Primary UDI-DI identifier for PowerCube+ Series?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is A.
What classification code is assigned to this device?
This device is registered under product classification code JEH.
Similar Classification Devices (JEH)
Other Devices by Ganshorn Medizin Electronic GmbH
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