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Cordis PRECISE PRO Rx Nitinol Stent System
Model / Serial
Model: Multiple lot numbers, Affected: Product manufactured between April 27, 2015 and November 22, 2015.
Manufacturer
Cordis Corporation
1 Event
Recall of Cordis PRECISE PRO Rx Nitinol Stent System
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Manufacturer
Cordis Corporation
Manufacturer Parent Company (2017)
Cardinal Health
Source
NZMMDSA
2 devices with a similar name
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Cordis Precise Pro RX Nitinol Stent System
Model / Serial
Product Description
Class III
Manufacturer
Cordis Cooperation
Cordis PRECISE PRO RX Nitinol Stent System (Carotid)
Model / Serial
Cordis PRECISE PRO RX Nitinol Stent System (Carotid) Multiple Catalogue Numbers affectedMultiple Lot Numbers affectedARTG Number: 149399
Product Classification
Cardiovascular Devices
Manufacturer
Johnson & Johnson Medical Pty Ltd
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