Is my product a medical device (MD)? To know if your medical product falls within the scope of the CE marking legislation you must ensure if the product is classified as a medical device as defined in Directive 93/42/EEC. In the Medical Devices Directive (93/42/EEC) a medical device is defined as:
Read more
CE marking on medical devices indicates that they comply with the applicable European legislation with regard to product safety. Part of the CE marking process is drafting the Instruction For Use (Hereafter: IFU). The IFU provides general information on the use of the medical device as well as safety information including warnings. The Medical Devices
Read more
India’s medical device industry has become a booming business. As one of the largest markets in Asia, the government’s health initiatives are increasing and expected to grow in the upcoming years. The country’s Union cabinet agreed to examine the standing committee’s recommendations to modernize medical device regulations.
Read moreE-cigarettes have been a topic of conversation lately since experts aren’t sure whether these electronic cigarettes are a harmful alternative for smoking. The vaporizer cigarettes are metal tubes that are designed to look like real cigarettes and contain a cartridge filled with a liquid that is vaporized by a battery-powered heating element. Manufacturers say
Read more
