China NMPA Product Recall - Dry aortic valve EDWARDS INSPIRIS RESILIA Aortic Valve

China NMPA product recall for Dry aortic valve EDWARDS INSPIRIS RESILIA Aortic Valve by Edwards Lifesciences LLC published May 08, 2024. Recall level: Level 3 Recall. The National Medical Products Administration (NMPA) issued an announcement on May 8, 2024, regarding

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Record Information

Company

Edwards Lifesciences LLC

Inspection Date

Unknown Date

Product Type

ID: f5d5c851-4649-4bf4-8531-dbf4d07816b2

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