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並前往https://www.fda.gov/medical-devices/medical-device-recalls/cordis-recalls-precise-pro-rx-us-carotid-system-due-risk-separation-device-during-use

Cordis Recalls Precise PRO Rx US Carotid System Due to ...

The system includes a metal (nitinol) self-expanding stent preloaded on a delivery catheter used to place the stent. Reason for Recall. Cordis ...

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