Ce Mark Medical Device Search

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Ce mark medical device search.

The directives outline the safety and performance requirements for medical devices in the european union eu. Mark on a medical device once it has passed a conformity assessment. The adoption in. The medical device ce marking process will change when europe s new medical device regulation mdr 2017 745 comes into force in may 2021.

You should not place a ce mark on your medical device if it is. It is a criminal offence to affix a ce mark to a product that is not compliant or offer it for sale. Examples of medical devices with an ancillary medicinal substance. These products fall under the medical devices legislation and must be ce marked.

Products carrying both the ce mark and uk ni mark cannot be placed on the eu market. The ce mark is a legal requirement to place a device on the market in the eu. The ukca certification does not apply. The healthcare industry is changing and we have the breadth of expertise to help you evolve with it.

Where a device has been assessed by a uk approved body the uk ni mark will accompany but not replace the ce mark. The ce mark on a product indicates that the manufacturer or importer of that product affirms its compliance with the relevant eu legislation and the product may be sold anywhere in the european economic area eea. Departments worldwide how government works get involved consultations statistics. Ce marking is the medical device manufacturer s claim that a product meets the essential requirements of all relevant european medical device directives.

Ce marking routes of class i medical devices class iia medical devices medical devices of class iia could be such as surgical gloves hearing aids diagnostic ultrasound machines etc. Hello i m wondering if there s a centralized publicly available list database of medical devices that have received the ce mark in europe thanks for helping.