Devices

Device Recall Profiler Balloon Catheter

Model / Serial
Lot 532109 (Use By 2013-12)
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution including the states of CA, GA, ID, MI, OH and PA.
Product Description
ANGIODYNAMICS PROFILER BALLOON DILATATION CATHETER, Catalog No./REF 16801101, BALLOON DIAMETER 4MM, BALLOON LENGTH 2 CM, CATHETER LENGTH 40 CM, STERILE, MANUFACTURED IN USA AngioDynamics 603 Queensbury Avenue, Queensbury, NY 12804 || Cardiovascular catheterization
Manufacturer
Angiodynamics Worldwide Headquarters
1 Event
- Recall of Device Recall Profiler Balloon Catheter

Manufacturer

Angiodynamics Worldwide Headquarters

Manufacturer Address
Angiodynamics Worldwide Headquarters, 14 Plaza Drive, Latham NY 12110-3421
Manufacturer Parent Company (2017)
AngioDynamics Inc
Source
USFDA

One device with a similar name

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Device Recall Profiler Balloon Catheter

Model / Serial
Lot 532794 (Use By 2013-12)
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution including the states of CA, GA, ID, MI, OH and PA.
Product Description
ANGIODYNAMICS PROFILER BALLOON DILATATION CATHETER, Catalog No./REF 16801105, BALLOON DIAMETER 5MM, BALLOON LENGTH 4 CM, CATHETER LENGTH 40 CM, STERILE, MANUFACTURED IN USA AngioDynamics 603 Queensbury Avenue, Queensbury, NY 12804 || Cardiovascular catheterization
Manufacturer
Angiodynamics Worldwide Headquarters

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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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