Devices

Arrow Ultra 8 IAB

Model / Serial
Lot Numbers: KF0118523 MF8092597 MF8103402 MF8114055 MF9014548 MF9046091 MF9056823 MF9057130 MF9078053 MF9088776 MF9099410 MF9109907
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution -- USA, Canada, Australia, Belgium, Czechoslovakia, Germany, Russia, Spain, Finland, France, Great Britain, Hungary, Italy, Netherlands, Poland, Saudi Arabia, Switzerland, Brazil, Australia, Chile, Colombia, Ecuador, India, Indonesia, Japan, Korea, Malaysia, Mexico, New Zealand, Panama, Peru, Philippines, Taiwan, Thailand, and Venezuela.
Product Description
Percutaneous Insertion Tray For Use with: Arrow Ultra 8 IAB (Intra Aortic Balloon) Catheters || Model: IAK-05845
Manufacturer
Arrow International, Inc., Division of Teleflex Medical Inc.
1 Event
- Recall of Arrow Ultra 8 IAB

Manufacturer

Arrow International, Inc., Division of Teleflex Medical Inc.

Manufacturer Address
Arrow International, Inc., Division of Teleflex Medical Inc., 9 Plymouth St, Everett MA 02149-1814
Manufacturer Parent Company (2017)
Teleflex Incorporated
Source
USFDA

One device with a similar name

Learn more about the data here

Arrow Ultra 8 IAB (Intra-Aortic Balloon) Catheter , 8 Fr, 30cc., Arrow Ultra 8 IAB (Intra-Aortic ...

Model / Serial
Product Classification
Cardiovascular Devices
Manufacturer
Arrow International Inc

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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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