Portrait Cssxb

Portrait Core Services Installation Software V1.1.0

Registry build 21.09.26
11manufacturers in China registered for this device type
1catalogue number
1510(k) clearance

Who Else Makes It

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

Chinese manufacturers registered for FDA product code DRG
Manufacturer City Province Registered as Device types
Amphenol Medical Technologies (Dongguan) Co., Ltd. Dongguan Guangdong Contract manufacturer 77
Linxens Healthcare (Tianjin) Co., Ltd. Jinnan District Tianjin Contract manufacturer 7
Dongguan CFE Electronic Co., Ltd. Dongguan Guangdong Contract manufacturer 2
Chero Technology Co., Ltd. Jiaxing Zhejiang Contract manufacturer 1
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70
Shenzhen Mindray BIO-Medical Electronics Co., Ltd. Shenzhen Guangdong Specification developer 61
Edan Instruments, Inc. Shenzhen Guangdong Contract manufacturer 56
Orantech Inc. Shenzhen Guangdong Contract manufacturer 40
Suzhou Prosteri Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 20
Avita (Wujiang) Co., Ltd. Wujiang Jiangsu Contract manufacturer 15
Hangzhou VivaLNK Medical Technology Co., Ltd. Hangzhou Zhejiang Exporter 4

Record

Regulatory record for Portrait Cssxb
Listed by GE Medical Systems Information Technologies, Inc., United States
FDA product code DRG
Device type Transmitters And Receivers, Physiological Signal, Radiofrequency
Device class Class 2
Regulation 21 CFR 870.2910
Establishment Specification developer, Repacker / relabeller, Manufacturer
510(k) K234130
Record published 2024-04-30
Record revised 2026-01-30 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries lot or batch number

Catalogue Numbers

Catalogue numbers for Portrait Cssxb
Catalogue number Size Status
CSSXB In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Vital Sync Covidien LP 29
Transmitters And Receivers, Physiological Signal, Radiofrequency Nihon Kohden Corp. 22
LifeSync LifeSync Corporation 18
Surveyor Patient Cable Mortara Instrument, Inc. 18
Isansys Isansys Lifecare, Ltd. 15
ZephyrLIFE Home Zephyr Technology Corporation 11
Transmitters And Receivers, Physiological Signal, Radiofrequency Nihon Kohden America, Inc. 9
InTouch Health Intouch Health, Inc. 7
UbiqVue LifeSignals, Inc. 6
X12+ Mortara Instrument, Inc. 5
Welch Allyn, Inc. Welch Allyn, Inc. 5
Ezypro ECG Recorder Sigknow Biomedical Co., Ltd. 3

Showing 12 of 211. All products under Transmitters And Receivers, Physiological Signal, Radiofrequency

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K790144 1979-02-23

Recalls Naming This Product

4 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Portrait Cssxb
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
GE Medical Systems Information Technologies, Inc. 510(k) number 2026-07-20 Class II Device Design Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults following the update and will not follow the alarm settings previously configured fo 23 units
GE Medical Systems Information Technologies, Inc. 510(k) number 2026-07-20 Class II Device Design Software issue may result in a loss of patient monitoring at the Hub and Central Viewer. In addition, all alarm settings could be reset to factory defaults following the update and will not follow the alarm settings previously configured fo 4 units
GE Medical Systems Information Technologies, Inc. 510(k) number 2026-07-10 Class II Software design Portrait Core Services Software version V1.2.0 Security Vulnerability 11 units
GE Medical Systems, LLC 510(k) number 2024-12-06 Class II Software design There is a software issue that can result in the loss of patient monitoring on the Portrait Central Viewer Application after 425 days of continuous run-time. 7 systems

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