Devices

Device Recall VSeries

Model / Serial
Part Number (P/N): 0998-00-1800-101 and 0998-00-1800-201 with software version 2.4.1.18 in use with 12-lead ECG Module, P/N:0998-00-1804-01 and 0998-00-1804-02.
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution - US including the states of Louisiana, New Jersey, Montana, South Carolina and Wyoming.
Product Description
V-Series Patient Monitoring System, Manufactured for Mindray DS USA, Inc. Used for monitoring of human physiological parameters. The V-Series Monitor also has the capability of performing IV Drug and Hemodynamic Calculations and interfacing with network devices.
Manufacturer
Mindray DS USA, Inc. dba Mindray North America
1 Event
- Recall of Device Recall VSeries

Manufacturer

Mindray DS USA, Inc. dba Mindray North America

Manufacturer Address
Mindray DS USA, Inc. dba Mindray North America, 800 MacArthur Blvd, Mahwah NJ 07430-2001
Manufacturer Parent Company (2017)
Shenzhen Mindray Bio-Medical Electronics Co. Ltd.
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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