gudid Primary ID: Central Station v1

CARESCAPE (UDI Central Station v1)

Manufactured by GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The CARESCAPE (Model/Catalog Number: Central Station v1) is a medical device manufactured by GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC.. This product is indexed under FDA Product Code / Category Classification CBQ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Central Station v1
Product Code / EMDN: CBQ
Device Name: ASSY CSCS V1 MP100D DESKTOP
Database Sync Date: 2026-08-09 09:35:17

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 CARESCAPE?

The registered manufacturer of record for CARESCAPE is GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC..

What is the Primary UDI-DI identifier for CARESCAPE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Central Station v1.

What classification code is assigned to this device?

This device is registered under product classification code CBQ.

Similar Classification Devices (CBQ)

Other Devices by GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC.

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