Vereos PET/CT System Upgrade

Catalogue number Vereos PET/CT System Upgrade, listed by Philips Medical Systems Nederland B.V., Netherlands, under System, Tomography, Computed, Emission. 4 manufacturers in China are registered for this product code.

Registry build 21.09.26
4manufacturers in China registered for this device type
1catalogue number
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Beijing (1), Shanghai (1), Guangdong (1).

Chinese manufacturers registered for FDA product code KPS
Manufacturer City Province Registered as Device types
GE Hangwei Medical Systems Co., Ltd. Beijing Beijing Specification developer 22
Shanghai United Imaging Healthcare Co., Ltd. Shanghai Shanghai Manufacturer 12
Siemens Shenzhen Magnetic Resonance Ltd. Shenzhen Guangdong Contract manufacturer 8
Neusoft Positron Medical Systems Co., Ltd. Shen Yang Liaoning Manufacturer 1

Record

Regulatory record for Vereos PET/CT System Upgrade
Listed by Philips Medical Systems Nederland B.V., Netherlands
FDA product code KPS
Device type System, Tomography, Computed, Emission
Device class Class 2
Regulation 21 CFR 892.1200
Establishment Contract manufacturer, Remanufacturer, Specification developer, Complaint-file establishment, Manufacturer, Exporter
Record published 2022-03-21
Record revised 2025-05-26 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries serial number

Catalogue Numbers

Catalogue numbers for Vereos PET/CT System Upgrade
Catalogue number Size Status
Vereos PET/CT System Upgrade In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
NeuroQ Syntermed, Inc. 11
Emory Cardiac Toolbox Syntermed, Inc. 10
Discovery GE Medical Systems, L.L.C. 7
uMI Shanghai United Imaging Healthcare Co., Ltd. 7
Brightonix Brightonix Imaging Inc. 6
UltraSPECT Ultraspect USA, LLC 5
Discovery G E Medical Systems Israel Ltd. 5
Veriton CT Spectrum Dynamics Medical Ltd. 5
Cardius 2 Digirad Corp. 4
Encompass™ SRS Fibreplast™ System Qfix 4
Veriton NM Spectrum Dynamics Medical Ltd. 3
Cedars-Sinai Cardiac Suite Cedars Sinai Medical Center 3

Showing 12 of 172. All products under System, Tomography, Computed, Emission

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K211764 2021-08-06
K210880 2021-05-19

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