International Medical Devices Database

Manufacturer Parent Company (2017)
Teleflex Incorporated
Manufacturers representative
Novamed S.A.R.L.
Source
RLMPH
1 Event
- Recall of FiberOptix Intra-Aortic Balloon

One device in the database

FiberOptix Intra-Aortic Balloon

Model / Serial

6 manufacturers with a similar name

Learn more about the data here

Arrow International, Inc., Division of Teleflex Medical Inc.

Manufacturer Address
Arrow International, Inc., Division of Teleflex Medical Inc., 9 Plymouth St, Everett MA 02149-1814
Manufacturer Parent Company (2017)
Teleflex Incorporated
Source
USFDA

Arrow International, Inc.

Manufacturer Parent Company (2017)
Teleflex Incorporated
Source
SMPA

Arrow International, Inc.

Manufacturer Parent Company (2017)
Teleflex Incorporated
Source
SATP

Arrow International, Inc.

Manufacturer Parent Company (2017)
Teleflex Incorporated
Source
SATP

Arrow International, Inc.

Manufacturer Parent Company (2017)
Teleflex Incorporated
Source
ORMPMDBP

One more

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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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