Synapse Select

The VidiStar PACS & DICOM Viewer Software system is a picture archiving and communications system (PACS) intended to be used as a networked Digital Imaging and Communications in Medicine…

Registry build 21.09.26

The VidiStar PACS & DICOM Viewer Software system is a picture archiving and communications system (PACS) intended to be used as a networked Digital Imaging and Communications in Medicine (DICOM) and non-DICOM information and data management system. The VidiStar PACS & DICOM Viewer Software is comprised of modular software programs that run on standard “off-the-shelf” personal computers, business computers, and servers running standard operating systems. VidiStar PACS & DICOM Viewer Software system is an image, data storage and display software that accepts DICOM data from laboratories, which support DICOM standard imaging data and structured reporting transfer(s). The system provides the capability to: organize images generated by OEM vendor equipment, perform digital manipulation, create graphical representations of anatomical areas, perform quantitative measurements, and create DICOM structure reports, all over the Internet.

10manufacturers in China registered for this device type
1catalogue number
2recalls on this code

Who Else Makes It

Concentrated in Guangdong (7), Shanghai (2), Jiangsu (1). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code DQK
Manufacturer City Province Registered as Device types
Amphenol Medical Technologies (Dongguan) Co., Ltd. Dongguan Guangdong Contract manufacturer 77
Jabil Circuit (Shanghai) Ltd. Shanghai Shanghai Contract manufacturer 31
Amphenol Alden Products Company Shenzhen Guangdong Contract manufacturer 24
Dongguan Ergotron Precision Technology Co., Ltd. Dongguan Guangdong Contract manufacturer 2
Shenzhen Mindray BIO-Medical Electronics Co., Ltd. Shenzhen Guangdong Specification developer 61
GE Medical Systems (China) Co., Ltd. Wuxi Jiangsu Contract manufacturer 57
Edan Instruments, Inc. Shenzhen Guangdong Contract manufacturer 56
Shenzhen BelterHealthMeasurementAndAnalysisTechnologyCo.,Ltd Shenzhen Guangdong Manufacturer 7
Philips (China) Investment Co., Ltd. Philips Healthcare – Shanghai CDC Shanghai Shanghai Specification developer 6
Shenzhen Carewell Electronics Co., Ltd. Shenzhen Guangdong Manufacturer 2

Record

Regulatory record for Synapse Select
Listed by Fujifilm Healthcare Americas Corporation, United States
FDA product code DQK
Device type Computer, Diagnostic, Programmable
Device class Class 2
Regulation 21 CFR 870.1425
Establishment Specification developer, Repacker / relabeller, Manufacturer
Record published 2018-09-27
Record revised 2026-02-16 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries manufacturing date

Catalogue Numbers

Catalogue numbers for Synapse Select
Catalogue number Size Status
4.X.X In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
EnSite™ St. Jude Medical 177
Computer, Diagnostic, Programmable St. Jude Medical 57
MediGuide™ St. Jude Medical 41
AcQMap Acutus Medical, Inc. 38
WorkMate Claris™ St. Jude Medical 35
iLab Ultrasound Imaging System Boston Scientific Corporation 32
Rhythmia™ Mapping System Boston Scientific Corporation 31
Sentinel Spacelabs Healthcare (Washington), Inc 28
Rhythmia HDx™ Boston Scientific Corporation 26
EnSite Precision™ St. Jude Medical 23
PathfinderSL Spacelabs Healthcare (Washington), Inc 22
Labsystem™ PRO Boston Scientific Corporation 19

Showing 12 of 228. All products under Computer, Diagnostic, Programmable

Recalls

2 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2015-02-04 Class II Software in the Use Environment Under certain circumstances the patient
Demographics in a report exported into the EMR may not match the demographics shown in the corresponding Synapse CV clinical report.
16 units 2018-09-20
2015-02-04 Class II Software in the Use Environment Measurement values in the EMR may not accurately reflect the actual measurement value on the Synapse Cardiovascular clinical report. 30 units 2018-09-20

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