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    CE Marking Specialists


    A South Wales based Product  Certification and training company, specialising in supporting small to medium enterprises in meeting their CE Marking obligations


  • Specialists in EMC and Low Voltage

    (Safety) Directives


    We specialise in European and Worldwide approvals.

  • Flexible, Professional, and Affordable Service


    We are a small organisation employing only

    highly experienced associates.

Category: News

New OJ List of Harmonised standards for MD Directive now published

Base: Council Directive 93/42/EEC of 14 June 1993 concerning medical devices
OJ L 169 of 12 July 1993
Modification:
  • Directive 93/68/EEC [CE Marking]
  • Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices
  • Directive 2000/70/EC of the European Parliament and of the Council of 16 November 2000 amending Council Directive 93/42/EEC as regards medical devices incorporating stable derivates of human blood or human plasma
  • Directive 2001/104/EC of the European Parliament and of the Council of 7 December 2001 amending Council Directive 93/42/EEC concerning medical devices
  • Directive 2007/47/EC of the European Parliament and of the Council of 5 September 2007 amending Council Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical devices, Council Directive 93/42/EEC concerning medical devices and Directive 98/8/EC concerning the placing of biocidal products on the market

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New standard for in-home power line communication apparatus BS EN 50561-3:2016

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What is power line communication?

A common example of this is the home power-line communication adapters commonly used to transfer broadband from one adapter plug to another anywhere in your home. It doesn’t suffer the problems associated with signal loss from walls and obstructions like WIFI. This makes it a great way to get internet from a source connection downstairs to an office upstairs, which normally would be to far away for WIFI signals to reach.

Its also popular in offices, apartments and hotels with some networks crossing across the threshold of properties via distribution networks and premises wiring. Typically transformers prevent propagating the signal, which requires multiple technologies to form very large networks.

Various data rates and frequencies are used in different situations.

 

What is BS EN 50561-3:2016 for?

In-home Power line communication apparatus (PLC) use the mains-electricity wiring in the home for communication by injecting differential-mode (DM) signals. However these signals have the potential to cause interference to the operation of radio or telecommunication apparatus.

To control this situation both radiated-emissions and conducted-emissions tests are now specified, and both are necessary as they control different things. EN 50561-3 applies to equipment that uses frequencies including those above 30 MHz in order to communicate. Procedures are given for the measurement of signals generated by the equipment and limits are specified within the frequency range 9 kHz to 400 GHz. No measurement is required at frequencies where no limits are specified.

The radiated emission requirements in this standard are not intended to be applicable to the intentional transmissions from a radio-transmitter as defined by the ITU, nor to any spurious emissions related to these intentional transmissions.

 

When is BS EN 50561-3:2016 coming out?

latest date by which this document has to be implemented at national level by publication of an identical national standard or by endorsement
(dop) 2016-11-23

latest date by which the national standards conflicting with this document have to be withdrawn
(dow) 2018-11-23

 

For more information contact us

 

Low Voltage Directive Transition from 2006/95/EC to 2014/35/EU

A Guidance document on the Low Voltage Directive transition from 2006/95/EC to 2014/35/EU is now available, with a list of frequently asked questions and answers.

This document is preliminary, pending finalisation of the revised Blue Guide (planned for end of 2015) and the LVD Guidelines (planned for mid-2016).

This document states:
“. . . . the main changes in the new Directive 2014/35/EU with respect to the previous Directive 2006/95/EC are quite limited, and do not concern the most substantial characteristics of the act that remain the same: scope, safety objectives, conformity assessment procedure.”
The main changes are the following:

 

  • New Directive reference number
  • Definitions updated in-line with the NLF
  • Economic operators, and their obligations, defined as:
  1. Manufacturers,
  2. Authorised representatives,
  3. Importers,
  4. Distributors
  • Harmonised standards and presumption of conformity: reference to Regulation (EU) No 1025/2012
  • CE marking: reference to Regulation (EC) No 765/2008
  • Market surveillance and safeguard procedure: reinforced activities and new simplified procedures
  • Commission Implementing Decisions on formal objections against harmonised standards and safeguard clauses against products: reference to Regulation (EU) No 182/2011
  • More detailed contents for the declaration of conformity, (Annex IV)