Sunquest Application Interfacing

Sunquest Application Interface (AI) is to provide interfaces between client systems and Sunquest products to support laboratories in the management of laboratory workflow (order entry…

Registry build 21.09.26

Sunquest Application Interface (AI) is to provide interfaces between client systems and Sunquest products to support laboratories in the management of laboratory workflow (order entry through reporting) and transfer test results and information

11manufacturers in China registered for this device type
1catalogue number

Who Else Makes It

Concentrated in Guangdong (4), Shanghai (3), Jiangsu (2). 5 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code OUG
Manufacturer City Province Registered as Device types
Edan Instruments, Inc. Shenzhen Guangdong Contract manufacturer 56
Jabil Circuit (Shanghai) Ltd. Shanghai Shanghai Contract manufacturer 31
Dongguan BAO Kang Dian ZI KE JI Limited Dongguan Guangdong Contract manufacturer 24
Primecare Medical (Suzhou) Co., Ltd. Changshu Jiangsu Contract manufacturer 20
Shenzhen Insighters Medical Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 10
Changshu Rozer Sterilization Technology Co., Ltd. Changshu Jiangsu Contract manufacturer 43
Hangzhou Primecare Medical Co., Ltd. Hangzhou Zhejiang Contract manufacturer 29
Shanghai Mediworks Precision Instruments Co., Ltd. Shanghai Shanghai Contract manufacturer 13
Zhejiang Yigao Medical Technology Co., Ltd. Hangzhou Zhejiang Manufacturer 7
Resvent Medical Technology Co., Ltd. Shenzhen Guangdong Contract manufacturer 6
Shanghai Draeger Medical Instrument Co., Ltd. Shanghai Shanghai Contract manufacturer 4

Record

Regulatory record for Sunquest Application Interfacing
Listed by CliniSys, Inc, United States
FDA product code OUG
Device type Medical Device Data System
Device class Class 1
Regulation 21 CFR 880.6310
Establishment Manufacturer
Premarket notification Exempt
Record published 2020-12-23
Record revised 2023-07-24 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries lot or batch number
Distribution end date 2021-10-29

Catalogue Numbers

Catalogue numbers for Sunquest Application Interfacing
Catalogue number Size Status
5.3 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Responder Rauland-Borg Corporation 170
Medical Device Data System Pentax of America, Inc. 72
DreamStation Respironics Inc. 55
Endopro IQ Pentax of America, Inc. 49
MonitAir Monitair, LLC 22
Medical Device Data System Medtronic, Inc. 20
DreamMapper Respironics Inc. 16
Arthrex® Arthrex, Inc. 14
Visionflex Visionflex PTY Limited 11
Intesys Clinical Suite Spacelabs Healthcare (Washington), Inc 11
myoncare Oncare GmbH 9
MicroScan Beckman Coulter, Inc. 9

Showing 12 of 281. All products under Medical Device Data System

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