International Medical Devices Database

Manufacturer Parent Company (2017)
Teleflex Incorporated
Source
NZMMDSA
1 Event
- Recall of Teleflex Athlone - OnControl Bone Marrow Systems

One device in the database

Teleflex Athlone - OnControl Bone Marrow Systems

Model / Serial
Model: , Affected: Catalogue numbers: 9403-EU-006, 9408-EU-006, 9411-EU-006, 9462-EU-001, 9463-EU-001, 9464-EU-001, 9466-EU-001

3 manufacturers with a similar name

Learn more about the data here

TELEFLEX MEDICAL EUROPE LTD

Manufacturer Parent Company (2017)
Teleflex Incorporated
Source
MSHM

Teleflex Medical Europe Ltd

Manufacturer Parent Company (2017)
Teleflex Incorporated
Source
LAANSM

Teleflex Medical Europe Ltd

Manufacturer Address
Teleflex Medical Europe Ltd, Ida Business Park, Athlone Ireland
Manufacturer Parent Company (2017)
Teleflex Incorporated
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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