In an era of increasingly stringent global medical device regulations, the EU MDR has been implemented for a year; the UK regulations are also starting to reform, and will implement similar requirements to the EU next year.

As a leading medical cart manufacturer in China, CORITON is currently the only medical cart manufacturer in China that has obtained the German TUV SUD ISO13485 certification. The most important aspect of ISO13485 implementation is compliance with relevant regulations.CORITON has now taken the lead in completing the latest MDR CE certification in the European Union; at the same time, it has also completed the UK UKCA certification, realizing support for the regulations of the European Union, the United Kingdom and the United States.

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?rid=200760

https://ec.europa.eu/tools/eudamed/#/screen/search-eo/2d0fd286-ddd2-4a11-a378-c300426da0e2

https://aic.mhra.gov.uk/era/pdr.nsf/Search?SearchView&Query=/era/pdr.nsf/Search?SearchView&Query=[ManName]Contains(%22coriton%22)&SearchOrder=4