Becton, Dickinson & Co. (BD) recalled intraosseous needle set kits and power drivers. The action was triggered by difficulties in separating the stylet from the needle. The FDA also announced a class ...
BD has begun a voluntary recall of many of its intraosseous needle kits and delivery systems, citing a handful of potential safety issues with the devices. Inserted through the bone to quickly deliver ...
BD (Becton, Dickinson and Co.) voluntary recalled certain lots of the BD Intraosseous Needle Set Kits, BD Intraosseous Manual Driver Kits and BD Intraosseous Powered Drivers, the Franklin Lakes ...
BD (Becton, Dickinson and Company), a leading global medical technology company, announced a voluntary recall on the BD Intraosseous Needle Set Kits, BD Intraosseous Manual Driver Kits and BDTM ...
Teleflex Corporation TFX recently announced that the FDA has granted 510(k) clearance to e Arrow EZ-IO Needle — the first and only intraosseous (IO) needle — for MR Conditional labeling. The ...
With 1000+ market research reports and 1 billion+ data points, Future Market Insights (FMI) serves each and every requirement of the clients operating in the global healthcare, pharmaceuticals, and ...
The following text summarizes information provided in the video. The medullary cavity is a highly vascular structure that functions as a noncollapsible vein capable of accepting a large volume of ...
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