gudid
Primary ID: V 5.0.0
MYSOZO.com (UDI V 5.0.0)
Manufactured by IMPEDIMED LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MYSOZO.com - Primary ID V 5.0.0
Device Regulatory Overview
The MYSOZO.com (Model/Catalog Number: V 5.0.0) is a medical device manufactured by IMPEDIMED LIMITED. This product is indexed under FDA Product Code / Category Classification DSB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- V 5.0.0
- Product Code / EMDN
- DSB
- Device Name
- Multipurpose software application- impedance analysis software that supports the measurement of extracellular fluid volume differences between the limbs and in the whole body, to track changes in the fluid state overtime; impedance analysis software utilizing impedance ratios that are displayed as an L-Dex ratio, that supports the measurement of extracellular fluid volume differences between the limbs and is presented to the clinician on an L-Dex scale.
- Database Sync Date
- 2026-08-09 09:43:49
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 MYSOZO.com?
The registered manufacturer of record for MYSOZO.com is IMPEDIMED LIMITED.
What is the Primary UDI-DI identifier for MYSOZO.com?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is V 5.0.0.
What classification code is assigned to this device?
This device is registered under product classification code DSB.
Similar Classification Devices (DSB)
Other Devices by IMPEDIMED LIMITED
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