International Medical Devices Database

Manufacturer Parent Company (2017)
Nihon Kohden Corp.
Source
MHM
1 Event
- Recall Or Safety Alert for DBP-2800 Battery Packs used in its Lifeline AED and ReviveR AED (semi-automatic external defibrillators)

One device in the database

DBP-2800 Battery Packs used in its Lifeline AED and ReviveR AED (semi-automatic external defibril...

Model / Serial
Product Classification
Cardiovascular Devices

3 manufacturers with a similar name

Learn more about the data here

DEFIBTECH LLC

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

Defibtech LLC

Manufacturer Address
Defibtech LLC, 4 Progress Ave, Seymour CT 06483-3921
Manufacturer Parent Company (2017)
Nihon Kohden Corp.
Source
USFDA

Defibtech LLC

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

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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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