eudamed_udi
Primary ID: 08809458500054
CUBEScan (UDI 08809458500054)
Manufactured by Mcube Technology Co., Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CUBEScan - Primary ID 08809458500054
Device Regulatory Overview
The CUBEScan (Model/Catalog Number: BioCon-2000W) is a medical device manufactured by Mcube Technology Co., Ltd. This product is indexed under FDA Product Code / Category Classification Z12062801 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BioCon-2000W
- Product Code / EMDN
- Z12062801
- Device Name
- Magnetic Incontinence Therapy System
- Database Sync Date
- 2026-08-09 16:30:30
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 CUBEScan?
The registered manufacturer of record for CUBEScan is Mcube Technology Co., Ltd.
What is the Primary UDI-DI identifier for CUBEScan?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08809458500054.
What classification code is assigned to this device?
This device is registered under product classification code Z12062801.
Similar Classification Devices (Z12062801)
Other Devices by Mcube Technology Co., Ltd
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