将通用医疗器械投放市场
作为医疗器械制造商，您必须在产品上市之前确保其满足相关法规要求。选择一家了解行业，并具有丰富评审经验的欧盟公告机构或英国授权机构至关重要。
BSI荷兰(2797)是全球领先的欧盟公告机构，我们对医疗器械进行评审以确保它们符合欧盟指令和法规的要求。BSI英国(0086)是英国授权机构，能够根据新的UKCA认证方案提供符合性评审。
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