About the database
How to use the database
Download the data
FAQ
Credits
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
{{ $t('card.reduce') }}
{{ $tc('card.more', left) }}
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
Learn more about the data
here
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
Language
English
Français
Español
한국어