International Medical Devices Database

Manufacturer Address
Gyrus ACMI Corporation, 136 Turnpike Road, Southborough MA 01772-2118
Source
USFDA
1 Event
- Recall of Device Recall Gyrus CyberWand

One device in the database

Device Recall Gyrus CyberWand

Model / Serial
Product distributed prior to May 7, 2007.
Product Classification
Gastroenterology-Urology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide and Canada.
Product Description
Gyrus CyberWand Ultrasonic Lithotripter System includes: || CW-USLS CyberWand USL System || CW-USLT CyberWand USL Transducer || CW-USLRBP CyberWand USL Renal/Bladder Probe Set || CW-USLTT CyberWand USL Transducer Sterilization Tray

2 manufacturers with a similar name

Learn more about the data here

Gyrus ACMI Corporation

Manufacturer Address
Gyrus ACMI Corporation, 136 Turnpike Rd, Southborough MA 01772-2118
Source
USFDA

Gyrus ACMI Corporation

Manufacturer Address
Gyrus ACMI Corporation, 136 Turnpike Road, Southborough MA 01772
Manufacturer Parent Company (2017)
Olympus Corporation
Source
USFDA

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Disclaimer

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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The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

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