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The Radio Equipment Directive (2014/53/EU) ensures a Single Market for radio equipment by setting essential requirements for safety and health, electromagnetic compatibility, and the efficient use of the radio spectrum.


It applies to all products using the radio frequency spectrum. It has been applicable since 13 June 2016. As of 13 June 2017 the new set of requirements of RED are applicable to the equipment.

According to RED directive, the conformity against the following requirements needs to be demonstrated:

  • 3.1(a): Radio equipment shall be constructed so as to ensure the protection of health and safety of persons and of domestic animals and the protection of property, including the objectives with respect to safety requirements set out in Directive 2014/35/EU (LVD), but with no voltage limit applying;
  • 3.1(b): Radio equipment shall be constructed so as to ensure an adequate level of electromagnetic compatibility as set out in Directive 2014/30/EU (EMC).
  • 3.2: Radio equipment shall be so constructed that it both effectively uses and supports the efficient use of radio spectrum in order to avoid harmful interference.

Starting with 20 December 2020 only the EN62368-1 will be accepted as a proof of conformity for LVD part of CE RED requirements.

Standards applied

The conformity with the essential requirements has been demonstrated against the following harmonized standards:

Standard Article
EN 60950–1:2006 + A1:2010 + A2:2013 + A11:2009 + A12:2011

IEC 60950–1:2005 (Second Edition) + A1:2009 + A2:2013

CSA C22.2 No. 60950–1:2007 + A1:2011 + A2:2014

UL60950-1:2007 (Second Edition) + A1:2011 + A2:2014

EN 62311:2008

EN 50383:2010

Health and safety - Article 3.1(a)
Draft EN 303 446-1 V1.1.0

Draft EN 301 489-1 V2.2.0

Draft EN 301 489-17 V3.2.0

Draft EN 301 489-52 V1.1.0

Electromagnetic compatibility - Article 3.1(b)
EN 301 511 V12.5.1

EN 301 908-1 V11.1.1

EN 301 908-2 V11.1.1

EN 301 908-13 V11.1.1

Draft EN 303 413 V1.1.0

EN 300 328 V2.1.1

Efficient use of radio spectrum - Article 3.2

Therefore   is placed on the product.


Test reports that are referenced in declarations and certificates can be provided upon request. For the request to be approved, the recipient of the test reports should be a certification authority or certified test house. The recipients will be asked to sign a non-disclosure agreement (NDA).


EU Declaration of conformity, FMA202 page 1
EU Declaration of conformity, FMA202 page 2

You can the find PDF version of the declaration here.

External links