China NMPA Product Recall - Intra-Aortic Occlusion Device
China NMPA product recall for Intra-Aortic Occlusion Device by Edwards Lifesciences LLC published August 09, 2019. Recall level: Level 1 Recall. The National Medical Products Administration (NMPA) issued an announcement on August 9, 2019, detail
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 Intra-Aortic Occlusion Device by Edwards Lifesciences LLC published August 09, 2019. Recall level: Level 1 Recall. The National Medical Products Administration (NMPA) issued an announcement on August 9, 2019, detail
Access our comprehensive regulatory intelligence platform to analyze patterns, track compliance trends, and stay ahead of regulatory changes.
Company
Edwards Lifesciences LLCInspection Date
Unknown Date
Product Type
ID: accb9387-12d4-4469-a572-f3b57a5ef84d
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