Ce Mark Medical Device Meaning

These products fall under the medical devices legislation and must be ce marked.

Ce mark medical device meaning.

It shows that the device is fit for its intended purpose stated and meets. Ce marking indicates that your medical device complies with the applicable eu regulations and enables the commercialization of your products in 32 european countries. A medical device may contain an ancillary medicinal substance to support the proper functioning of the device. The ce mark is a legal requirement to place a device on the market in the eu.

How to determine if your product requires a ce mark in the eu if you want to know whether your product is considered a medical device in the eu and if you want to know the definition of a medical device in the eu do read on. Ce marking is an administrative marking that indicates conformity with health safety and environmental protection standards for products sold within the european economic area eea. Ce marking is the medical device manufacturer s claim that a product meets the essential requirements of all relevant european medical device directives. The answer to what may appear to be a simple question is in some cases quite complex.

To facilitate trade throughout the european economic area eea products need to be identified as compliant with regional and national regulations. The directives outline the safety and performance requirements for medical devices in the european union eu. This makes the ce marking recognizable. Ce marking is the medical device manufacturer s claim that a product meets the essential requirements of all relevant european medical device directives.

As a legal medical device manufacturer you are responsible for maintaining regulatory compliance and securing ce marking for your product regardless of whether you outsource any. The author answers the question of what does the ce mark means what its purpose is related to medical devices and regulatory requirements if applicable. The directives outline the safety and performance requirements for medical devices in the european union eu. The ce mark is a legal requirement to place a device on the market in the eu.

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.