Ce Mark Medical Device Database Search

Eudamed is the it system developed by the european commission to implement regulation eu 2017 745 on medical devices and regulation eu 2017 746 on in vitro diagnosis medical devices.

Ce mark medical device database search.

Instead only the eu national regulators will have access. Ce marking applies to products ranging from electrical equipment to toys and from civil explosives to medical devices. Hello i m wondering if there s a centralized publicly available list database of medical devices that have received the ce mark please sign up sign in to read the entire article. A medical device may contain an ancillary medicinal substance to support the proper functioning of the device.

The new regulations contain important improvements including a much larger eudamed database than the one that currently exists under the medical devices directives. Here we can include medical devices such as long term corrective contact lenses surgical lasers defibrillators and others. We invite you to search the tris database using the options bellow. These products fall under the medical devices legislation and must be ce marked.

The full list of these product categories is below. But it will be introduced by the incoming medical device regulations. Please be aware that complex searches will take longer to perform. You are welcome to choose any combination of filters.

In addition the following fact databases are available for general search within the medical devices information system public part. Class iib medical devices. The full list of these. Prepare a declaration of conformity doc which states that your device complies with the appropriate directive.

Is there any database for list of ce marked medical devices and there current sta such a database does not exist. Examples of medical devices with an ancillary medicinal substance include drug eluting stents bone cement containing an antibiotic catheters coated with heparin or an antibiotic agent and condoms coated. Obtain ce marking and iso 13485 certificates from your notified body. Ce marking routes of class iia medical devices.

The medical device ce marking process will change when europe s new medical device regulation mdr 2017 745 comes into force in may 2021. There are four possible routes to ce mark your product split into two groups given the product s type i e if it s sterile or not.