European Commission changes stance on CE-marking
This article was originally published in Clinica
Executive Summary
In response to industry pressure, the European Commission has decided that non-CE marked medical devices may be sold after the medical device directives become mandatory in the European Economic Area on June 14th, 1998. If the device is already in the distribution chain by that date, but not CE-marked, it will now be marketable until June 2001.
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