China NMPA Product Recall - Medtronic PRO+ Transcatheter Aortic Valve System

China NMPA product recall for Medtronic PRO+ Transcatheter Aortic Valve System by Medtronic Inc. published June 04, 2025. Recall level: Level 3 Recall. The National Medical Products Administration (NMPA) published an announcement on June 4, 2025, regar

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Record Information

Company

Medtronic Inc.

Inspection Date

Unknown Date

Product Type

ID: e5b36415-1461-4cef-b640-084a5fb49333

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