Automation Platform

The Automation Platform is a software product that transfers, stores, converts formats, and displays medical device image data. It does not modify the image data or modify the display of…

Registry build 21.09.26

The Automation Platform is a software product that transfers, stores, converts formats, and displays medical device image data. It does not modify the image data or modify the display of the image data. The Automation Platform reads images and interprets DICOM tags, analyzes pixels to identify body part and sequence type in order to categorize the images. The Automation Platform is not intended to be used for active patient monitoring nor primary image interpretation. The Automation Platform allows routing DICOM-compliant image data to and from automated post processing applications, but such processing applications are not a part of the platform itself. Automation Platform allows post processing applications to provide a notification or a flag intended to inform the user.

6manufacturers in China registered for this device type
1catalogue number

Who Else Makes It

Concentrated in Jiangsu (4), Tianjin (1), Beijing (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code LMD
Manufacturer City Province Registered as Device types
Coretronic Projection (Kunshan) Corporation Kunshan Jiangsu Contract manufacturer 3
AUO (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 1
Nanjing Jusha Display Technology Co., Ltd. Nanjing Jiangsu Manufacturer 7
Barco (Suzhou) Healthcare Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 4
Beijing Visual Perception Intelligence Technology Co., Ltd. Tianjin Tianjin Manufacturer 1
E-COM Technology Co., Ltd. Beijing Beijing Manufacturer 1

Record

Regulatory record for Automation Platform
Listed by Olea Medical USA
FDA product code LMD
Device type System, Digital Image Communications, Radiological
Device class Class 1
Regulation 21 CFR 892.2020
Premarket notification Exempt
Record published 2019-11-25
Record revised 2023-10-18 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries lot or batch number
Distribution end date 2020-11-30

Catalogue Numbers

Catalogue numbers for Automation Platform
Catalogue number Size Status
1.0 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Vitrea Advanced Visualization Canon Medical Informatics, Inc. 34
Barco Barco, Inc 27
RadiForce® Eizo Corporation 23
Vitrea Read Canon Medical Informatics A/S 19
Image Diagnostics, Inc Image Diagnostics, Inc. 19
ScaleOR NDS Surgical Imaging, LLC. 17
interWORKS Avreo, Inc. 16
Vitrea View Canon Medical Informatics, Inc. 14
Clinical review 2MP Barco, Inc 11
Barco Fimi SRL 10
Super Ulstar Durico C&T, Inc. 9
VISIUSmatrix Imris Imaging, Inc. 9

Showing 12 of 193. All products under System, Digital Image Communications, Radiological

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer