This is done under the responsibility of the Notified Body.

Any system selected and installed, should be certified by a notified body.

To find out about notified bodies, see the page in this guide on legal and regulatory activities.

Products considered to have a greater risk have to be independently certified by a notified body.

If a Notified Body was involved in the production control phase, its identification number must also be displayed.

If a Notified Body validates your product, the mark must also carry the body's identification number.

Where relevant, it should be accompanied by the identification number of the Notified body that carried out the conformity assessment procedures.

As a notified body, it can issue:

To do this, you need to ensure that the fireworks have been tested by a notified body (NB).

Actuators designed for these applications, being explosion-proof devices, have to be qualified by a test authority (notified body).

Find a local notified body to evaluate your weighing/measuring equipment with the NMO.

However, you should note that the NMO is not a notified body for gas and electricity meters.

Lists of notified bodies for various EU directives.

I said at first reading that the principle of independence for notified bodies would be set out in Annex C of the measure.

Before 2004, had the responsibility as a Notified Body for the use of the CE mark on dental products.

This is not obligatory for all products, so it is important to check whether the involvement of a Notified Body is indeed required.

You may also have to get confirmation of satisfactory testing, inspection or quality assessment from an officially recognised organisation (referred to as a Notified Body).

Its products have a CE mark, which means they have been quality-approved by a "notified body" in Europe.

Oversee the Notified Bodies that ensure medical device manufacturers comply with regulatory requirements before putting devices on the market.

Organisations called Notified Bodies are accredited by the EU to assess the devices and their makers.

The use of safety devices for safety applications usually requires the certification of the devices by notified bodies.

If stipulated in the directive(s), an authorized third party (Notified Body) must be involved in the conformity assessment procedure.

Following manufacture, a technical file and Notified Body certificate will be obtained on completion of a manufacturing and maintenance procedures review.

A Notified Body is a public or private organisation that has been accredited to validate the compliance of the device to the European Directive.

That is what has happened in the common position which states that a notified body must be independent and not be controlled by manufacturers or by suppliers.