International Medical Devices Database

Manufacturer Parent Company (2017)
Philips
Source
AEMPSVFOI
1 Event
- Recall Or Safety Alert for Trilogy fans 100, 200 and 202, software version 13.2.04, 13.2.05, 14.0.00 or 14.1.01 and with the double prescription enabled.

One device in the database

Trilogy fans 100, 200 and 202, software version 13.2.04, 13.2.05, 14.0.00 or 14.1.01 and with the...

Model / Serial

5 manufacturers with a similar name

Learn more about the data here

Philips Respironics Inc.

Manufacturer Parent Company (2017)
Philips
Source
SATP

Philips Medical Systems Ltda.; Respironics Inc.

Manufacturer Parent Company (2017)
Philips
Source
ANVSANVISA

VR Medical Importadora e Distribuidora de Produtos Médicos; Respironics Inc. (Currently Philips R...

Source
ANVSANVISA

RESPIRONICS INC.

Manufacturer Address
MURRYSVILLE
Manufacturer Parent Company (2017)
Philips
Source
HC

Respironics Inc.

Manufacturer Parent Company (2017)
Philips
Source
MHM

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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