Devices

Device Recall DUOSTAT

Model / Serial
6090551
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide, including USA, Canada, Germany, Italy, Greece, New Zealand, Netherlands, France, Japan, Spain, and Bulgaria.
Product Description
ACS DUOSTAT¿ Rotating Hemostatic Valve, 0.096 inch, for use with a dilatation catheter - Reference Number 23244
Manufacturer
Abbott Vascular-Cardiac Therapies dba Guidant Corporation
1 Event
- Recall of Device Recall DUOSTAT

Manufacturer

Abbott Vascular-Cardiac Therapies dba Guidant Corporation

Manufacturer Address
Abbott Vascular-Cardiac Therapies dba Guidant Corporation, 26531 Ynez Rd, Temecula CA 92591-4630
Source
USFDA

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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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