![]() ![]() The term “CE” is the short form of the French phrase “Conformité Européene,” which translates to “European Conformity” in English. If the medical device is imported from outside the EEA, then this obligation transfers to the importer. ![]() It is the producer’s mandatory obligation to acquire and display the CE mark on the device before marketing it in the European Economic Area (EEA). The CE marking is a gateway to marketing products in Europe, even if the medical device was produced somewhere other than the European Union.
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