China NMPA Product Recall - HL888UF Upper Arm Electronic Blood Pressure Monitor
China NMPA product recall for HL888UF Upper Arm Electronic Blood Pressure Monitor by Holtek Medical Electronics (Suzhou) Co., Ltd. published March 15, 2019. Recall level: Level 3 Recall. Holtek Medical Electronics (Suzhou) Co., Ltd., also identified as HeTai Medical Electronics Suzhou C
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 HL888UF Upper Arm Electronic Blood Pressure Monitor by Holtek Medical Electronics (Suzhou) Co., Ltd. published March 15, 2019. Recall level: Level 3 Recall. Holtek Medical Electronics (Suzhou) Co., Ltd., also identified as HeTai Medical Electronics Suzhou C
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