gudid
Primary ID: V2.76
ReDS Pro System (UDI V2.76)
Manufactured by SENSIBLE MEDICAL INNOVATIONS LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ReDS Pro System - Primary ID V2.76
Device Regulatory Overview
The ReDS Pro System (Model/Catalog Number: V2.76) is a medical device manufactured by SENSIBLE MEDICAL INNOVATIONS LTD. This product is indexed under FDA Product Code / Category Classification DSB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- V2.76
- Product Code / EMDN
- DSB
- Device Name
- Fluid status monitor This catalog item is used by a health care provider in the hospital, hospital like facilities and home setting
- Database Sync Date
- 2026-08-09 09:18:12
Full Regulatory Attributes
🔒 Token Gated
{
"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 ReDS Pro System?
The registered manufacturer of record for ReDS Pro System is SENSIBLE MEDICAL INNOVATIONS LTD.
What is the Primary UDI-DI identifier for ReDS Pro System?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is V2.76.
What classification code is assigned to this device?
This device is registered under product classification code DSB.
Similar Classification Devices (DSB)
Other Devices by SENSIBLE MEDICAL INNOVATIONS LTD
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