Unrivalled expertise from an EU Notified Body and UK Approved Body

Our ophthalmic technical specialists have extensive experience and can support you through the process of certifying your ophthalmic medical device.

As a manufacturer of an ophthalmic medical device, you must ensure that you meet the relevant regulatory requirements before placing your product onto the market; for the EU, these are outlined in the Medical Device Regulation (MDR) (EU) 2017/745 and, for the UK, the UK Medical Devices Regulations (UK MDR) 2002.




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