International Medical Devices Database

Manufacturer Parent Company (2017)
Teleflex Incorporated
Source
LAANSM
1 Event
- Recall of Twin-Pass Vascular Catheters;Twin-Pass RX

One device in the database

Twin-Pass Vascular Catheters;Twin-Pass RX

Model / Serial
Product Classification
Cardiovascular Devices
Product Description
medical_device

19 manufacturers with a similar name

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Vascular Solutions, Inc.

Manufacturer Address
Vascular Solutions, Inc., 6464 Sycamore Ct N, Maple Grove MN 55369-6032
Manufacturer Parent Company (2017)
Teleflex Incorporated
Source
USFDA

Guidant Endovascular Solutions, Inc.

Manufacturer Address
Guidant Endovascular Solutions, Inc., 26531 Ynez Rd, Temecula CA 92591-4630
Source
USFDA

Vascular Solutions, Inc

Manufacturer Parent Company (2017)
Teleflex Incorporated
Source
AEMPSVFOI

Vascular Solutions, Inc.

Manufacturer Parent Company (2017)
Teleflex Incorporated
Source
AEMPSVFOI

Vascular Solutions, Inc., USA

Manufacturer Parent Company (2017)
Teleflex Incorporated
Source
NOM

14 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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