China NMPA Product Recall - Intra-Aortic Occlusion Device
China NMPA product recall for Intra-Aortic Occlusion Device by Edwards Lifesciences LLC published May 23, 2019. Recall level: Level 1. Edwards Lifesciences LLC, the manufacturer, in conjunction with its agent, Edwards (Shanghai) Medica
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China NMPA product recall for Intra-Aortic Occlusion Device by Edwards Lifesciences LLC published May 23, 2019. Recall level: Level 1. Edwards Lifesciences LLC, the manufacturer, in conjunction with its agent, Edwards (Shanghai) Medica
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Company
Edwards Lifesciences LLCInspection Date
Unknown Date
Product Type
ID: dfbbefca-64b3-4978-bcdc-9e2897c62bf6
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