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3 个月内
BRIEF-Teleflex receives FDA 510(k) clearance for Arrow AC3 Optimustm Intra-Aortic Balloon Pump
2017年5月2日 / 上午11点18分 / 3 个月内

BRIEF-Teleflex receives FDA 510(k) clearance for Arrow AC3 Optimustm Intra-Aortic Balloon Pump

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May 2 (Reuters) - Teleflex Inc

* Teleflex receives fda 510(k) clearance for the arrow® ac3 optimustm intra-aortic balloon pump (iabp)

* Teleflex receives fda 510(k) clearance for the arrow® ac3 optimustm intra-aortic balloon pump (iabp)

* Teleflex inc- ac3 optimus iabp will be launched at two scientific meetings in may Source text for Eikon: Further company coverage:

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