gudid Primary ID: 4.1

Prism Flow (UDI 4.1)

Manufactured by PRISM CLINICAL IMAGING, INC.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Prism Flow (Model/Catalog Number: 4.1) is a medical device manufactured by PRISM CLINICAL IMAGING, INC.. This product is indexed under FDA Product Code / Category Classification LMD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 4.1
Product Code / EMDN: LMD
Device Name: Prism Flow is the DICOM communications and storage and Prism workflow manager. It provides integrated access, application configuration, and audit logging across physical locations and the cloud. The dedicated DICOM store holds raw, intermediate and processed results, as well as providing DICOM interoperability with scanners, PACS, treatment planning, and surgical navigation systems through powerful configurable sender/receiver and forwarding functions.
Database Sync Date: 2026-08-09 09:18:01

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 Prism Flow?

The registered manufacturer of record for Prism Flow is PRISM CLINICAL IMAGING, INC..

What is the Primary UDI-DI identifier for Prism Flow?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 4.1.

What classification code is assigned to this device?

This device is registered under product classification code LMD.

Similar Classification Devices (LMD)

Other Devices by PRISM CLINICAL IMAGING, INC.

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