China NMPA Product Recall - Intra-aortic occlusion catheter
China NMPA product recall for Intra-aortic occlusion catheter by Edwards Lifesciences LLC published November 06, 2018. Recall level: Level 3 Recall. On November 6, 2018, the National Medical Products Administration (NMPA) announced a Class III volun
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China NMPA product recall for Intra-aortic occlusion catheter by Edwards Lifesciences LLC published November 06, 2018. Recall level: Level 3 Recall. On November 6, 2018, the National Medical Products Administration (NMPA) announced a Class III volun
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Company
Edwards Lifesciences LLCInspection Date
Unknown Date
Product Type
ID: 89a8aa5d-db8c-43d9-881c-d2c2786fefab
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