For CE marking, European Union directives mention Market Survelliance Authorities. Each country has its own authority. You can reach the list of Market Survelliance Authorities for Radio Equipment Directive (RED, 2014/53/EU) from this official page of...
Radio Equipment Directive (RED, 2014/53/EU) is one of the directives published by European Union regulating the compliance of radio equipments. For CE marking of radio equipments, RED is one of the essential directives. RED ensures a single market for radio equipment...
The Food and Drug Administration (FDA) regulates medical devices in USA. FDA has established classifications for about 1700 generic types of devices and grouped them into sixteen medical specialties referred to as panels. Each of these generic types of devices is...
Every product needs testing prior to marketing it. EMC testing is one of the essential tests for products which are subjected to Electromagnetic Compatibility regulations. The neccessaity of EMC testing can be compared at product’s different stages. Products follow...
Radiated Emission , in other words, by means of Radiated Propagation is only one of the Electromagnetic Compatibility (EMC) tests. According to the product to be tested according to the EMC standard is determined after determining an anechoic chamber (anechoic...
Recent Comments