Devices

PRECISE PRO RX Nitinol Stent System

Model / Serial
see FSN | see FSN
Product Description
MD: Bare-metal carotid artery stent
Manufacturer
Cordis Corporation
1 Event
- Field Safety Notices about PRECISE PRO RX Nitinol Stent System

Manufacturer

Cordis Corporation

Manufacturer Parent Company (2017)
Cardinal Health
Source
SATP

6 devices with a similar name

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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

Cordis Precise Pro RX Nitinol Stent System

Model / Serial
Product Description
Class III
Manufacturer
Cordis Cooperation

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

PRECISE PRO RX Nitinol Stent System

Model / Serial
Implanted device?
Yes
Product Description
Non-active implants - special implants
Manufacturer
Cordis

Precise Pro RX Nitinol Stent System (Carotid)

Model / Serial
Product Description
Medical Device Safety Alert: Cordis Precise Pro RX Nitinol Stent System (Carotid)
Manufacturer
Cordis Corporation

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Disclaimer

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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