China NMPA Product Recall - Anterograde perfusion cannulation Cardioplegia Delivery Cannula
China NMPA product recall for Anterograde perfusion cannulation Cardioplegia Delivery Cannula by Medtronic Inc. published July 31, 2025. Recall level: Level 1 Recall. The National Medical Products Administration (NMPA) has issued an announcement regarding a supplemen
One-time purchase from the GKS catalog. Lifetime access in your library. Single documents and full company profiles available. All sales final.
China NMPA product recall for Anterograde perfusion cannulation Cardioplegia Delivery Cannula by Medtronic Inc. published July 31, 2025. Recall level: Level 1 Recall. The National Medical Products Administration (NMPA) has issued an announcement regarding a supplemen
Access our comprehensive regulatory intelligence platform to analyze patterns, track compliance trends, and stay ahead of regulatory changes.
Company
Medtronic Inc.Inspection Date
Unknown Date
Product Type
ID: 789103be-f2fe-46e5-9ee2-c12ac96c6c93
View on DashboardTransform Regulatory Data into Actionable Intelligence
Join leading pharmaceutical and medical device companies who trust GKS for their regulatory compliance needs.
Try KeyPedia Today
Explore our real use cases and discover our features in depth.
Subscribe to our newsletter
Get the latest updates and insights delivered to your inbox