International Medical Devices Database

Manufacturer Parent Company (2017)
Philips
Source
LAANSM
1 Event
- Recall of Turbo Elite Coronary Atherectomy Catheters and ELCA

One device in the database

Turbo Elite Coronary Atherectomy Catheters and ELCA

Model / Serial
Product Description
medical_device

11 manufacturers with a similar name

Learn more about the data here

SPECTRANETICS CORPORATION

Manufacturer Parent Company (2017)
Philips
Source
MSHM

Spectranetics Corporation

Manufacturer Parent Company (2017)
Philips
Source
FSSH

Spectranetics Corporation

Manufacturer Address
Spectranetics Corporation, 9965 Federal Drive, Colorado Springs CO 80921-3617
Manufacturer Parent Company (2017)
Philips
Source
USFDA

Spectranetics Corporation

Manufacturer Parent Company (2017)
Philips
Source
BAM

Spectranetics Corporation

Manufacturer Address
Spectranetics Corporation, 96 Talamine Ct, Colorado Springs CO 80907-5159
Manufacturer Parent Company (2017)
Philips
Source
USFDA

6 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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