Devices

ULTRAFLEX INTRA-AORTIC BALLOON

Model / Serial
Model Catalog: IAB-06840-U (Lot serial: > 100 numbers contact mfg); Model Catalog: IAB-05830-LWS (Lot serial: > 100 numbers contact mfg); Model Catalog: IAB-05840-LWS (Lot serial: > 100 numbers contact mfg); Model Catalog: IAB-06830-U (Lot serial: > 100 numbers contact mfg); Model Catalog: IAB-05830-U (Lot serial: > 10 numbers contact mfg); Model Catalog: IAB-05840-U (Lot serial: > 10 numbers contact mfg); Model Catalog: IAK-06845 (Lot serial: > 10 numbers contact mfg)
Product Classification
Cardiovascular Devices
Product Description
ULTRAFLEX INTRA-AORTIC BALLOON;ULTRA 8 INTRA-AORTIC BALLOON - LIGHTWAVE SENSOR;ULTRA IAB CATHETER KIT;PERCUTANEOUS INSERTION KIT
Manufacturer
TELEFLEX MEDICAL CANADA INC.
1 Event
- Recall of ULTRAFLEX INTRA-AORTIC BALLOON

Manufacturer

TELEFLEX MEDICAL CANADA INC.

Manufacturer Address
MARKHAM
Manufacturer Parent Company (2017)
Teleflex Incorporated
Source
HC

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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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