gudid Primary ID: V2.6

ReDS System (UDI V2.6)

Manufactured by SENSIBLE MEDICAL INNOVATIONS LTD

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The ReDS System (Model/Catalog Number: V2.6) 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: V2.6
Product Code / EMDN: DSB
Device Name: Fluid Status Monitor
Database Sync Date: 2026-08-09 09:18:12

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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Frequently Asked Questions

Who is the primary manufacturer of ReDS System?

The registered manufacturer of record for ReDS System is SENSIBLE MEDICAL INNOVATIONS LTD.

What is the Primary UDI-DI identifier for ReDS System?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is V2.6.

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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