International Medical Devices Database

Manufacturer Parent Company (2017)
Nihon Kohden Corp.
Source
DH
1 Event
- Safety Alert for Lifeline AED, ReviveR AED and Lifeforce AED

One device in the database

Lifeline AED, ReviveR AED and Lifeforce AED

Model / Serial
Product Description
Press release: Alert on voluntary recall and corrective action by Defibtech on semi-automatic external defibrillators

9 manufacturers with a similar name

Learn more about the data here

Defibtech, LLC

Manufacturer Address
Defibtech, LLC, 741 Boston Post Rd Ste 201, Guilford CT 06437-2714
Source
USFDA

Defibtech

Manufacturer Parent Company (2017)
Nihon Kohden Corp.
Source
BAM

Defibtech, LLC

Manufacturer Parent Company (2017)
Nihon Kohden Corp.
Source
SATP

Defibtech, LLC

Manufacturer Parent Company (2017)
Nihon Kohden Corp.
Source
ORMPMDBP

DEFIBTECH LLC

Manufacturer Address
GUILFORD
Manufacturer Parent Company (2017)
Nihon Kohden Corp.
Source
HC

4 more

About this database

Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

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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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