China NMPA Product Recall - External defibrillator monitor
China NMPA product recall for External defibrillator monitor by Philips Kincoway (Shenzhen) Industrial Co., Ltd. published April 19, 2021. Recall level: Level 2 Recall. Philips Kinco (Shenzhen) Industrial Co., Ltd. initiated a voluntary Class II recall of its Efficia D
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 External defibrillator monitor by Philips Kincoway (Shenzhen) Industrial Co., Ltd. published April 19, 2021. Recall level: Level 2 Recall. Philips Kinco (Shenzhen) Industrial Co., Ltd. initiated a voluntary Class II recall of its Efficia D
Access our comprehensive regulatory intelligence platform to analyze patterns, track compliance trends, and stay ahead of regulatory changes.
Transform 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