International Medical Devices Database

Manufacturer Parent Company (2017)
Smiths Group Plc
Source
SATP
1 Event
- Field Safety Notices about Portex Blue Line Ultra

One device in the database

Portex Blue Line Ultra

Model / Serial
100/813/080, 100/813/085, 100/813/090, 100/823/080, 100/833/090 | 1293472, 1293475, 1293476, 1293480, 1293485
Product Description
MD: Tracheostomy tube, clinical-use, single-use

122 manufacturers with a similar name

Learn more about the data here

Smiths Medical Asd, Inc.

Manufacturer Parent Company (2017)
Smiths Group Plc
Source
NIDFSINVIMA

Smiths Medical Md, Inc

Manufacturer Parent Company (2017)
Smiths Group Plc
Source
NIDFSINVIMA

Smiths Medical International Ltd (UK)

Manufacturer Parent Company (2017)
Smiths Group Plc
Source
NZMMDSA

Smiths Medical ASD Inc

Manufacturer Parent Company (2017)
Smiths Group Plc
Source
NZMMDSA

Smiths Medical MD Inc

Manufacturer Parent Company (2017)
Smiths Group Plc
Source
NZMMDSA

117 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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