China NMPA Product Recall - Subcutaneous implantable cardioverter defibrillator
China NMPA product recall for Subcutaneous implantable cardioverter defibrillator by Boston Scientific (BSC) published December 03, 2020. Recall level: Level 2 Recall. The National Medical Products Administration (NMPA) announced on December 3, 2020, a voluntary Class
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 Subcutaneous implantable cardioverter defibrillator by Boston Scientific (BSC) published December 03, 2020. Recall level: Level 2 Recall. The National Medical Products Administration (NMPA) announced on December 3, 2020, a voluntary Class
Access our comprehensive regulatory intelligence platform to analyze patterns, track compliance trends, and stay ahead of regulatory changes.
Company
Boston Scientific (BSC)Inspection Date
Unknown Date
Product Type
ID: c6a584cc-df52-4119-a031-4e2de29388ef
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