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1. V alert the user to potential restrictions or requirements for authorisation of use in certain MS such information shall be completed in the instructions accompanying RE The Commission may specify how to present this information 29 The DoC shall be a complete copy of the original be packed with each RE Not for EMCD LVD have the model structure and it shall be continuously updated be translated into the language s required by the MS tn which market the apparatus Is placed or made available 30 Copy of full EU DoC shall accompany each RE This may be replaced by a simplified EU DoC accompanying each RE If a simplified EU DoC is provided it shall be directly followed by the exact internet or e mail address where the full EU DoC can be obtained 31 Simplified EU DoC shall contain the following text Hereby aaaaa declares that the RE type designation of type of RE is in compliance with RED 2014 53 EU The full text of the EU DoC is available at the following internet address It shall be translated into the language s required by the MS in which market the RE is placed or made available copies of simplified DoC can be found in each language version of the RED or on EC website 32 1 Save paper by providing only the simplified DoC text in the product package On your website you then store the Full DoC tn all the necessary
2. not issue Reports amp Certificates with RED reference RED Radio Equipment Directive 2014 53 EU Main elements Applicable from 13 June 2016 Transitional period 13 6 2016 13 6 2017 Has a changed scope e New Frequency range lt 3000 GHz Some specific extra new requirements New Requirements to bring RED in line with the NLF requirements similar to EmcD Lvp Module A and Module H assessment e New Module B C assessment Change of Scope Definition of RE Essential requirements Provisions for Software Defined Radio Registration scheme for certain RE Extra information in user manual e Simplified DoC allowed e Geographical information in package New Conformity Assessment Procedures NB ID number only if Module H is used e Additional formal non compliances Deleted Items in the RED compared to R amp TTED ing In manual only needs to be on product and packaging But RED product must be accompanied A by a copy of the EU DoC or by a D simplified EU DoC TEXT not applicable for EMCD or LVD aay EU Member States have to use the ERO Frequency Information System EFIS set up by the European Radiocommunications Office ERO in order to make information on the use of spectrum in each MS available to the public e RE Manufacturers can then search in EFIS and evaluate whether and under which conditions RE may be used wit
3. D to be developed compliance requirements for a Radio Module and the Final Product that integrates a Radio Module will address this issue in detall RED Conformity Assessment Procedures ee e aspects la 1b 2 and 3 HS fully aiea gt No P Module B C Mandatory NB use Module A standard route ANNEX II choose the O Module B C NB use Se Module H NB use ANNEX IV NEW Manufacturer can always or Module H Mandatory NB Use RE can be built into products that are also under the scope of other Directives This may lead to other requirements naving preference Zz mae Examples of such other Directives Toy Directive Medical Equipment Directive Question The RED allows the CE marking to be smaller than 5 mm What if have a radio controlled Toy Answer You need to follow all applicable Directives RED and ToyD to your product The ToyD does not allow CE marking less than 5 mm so A eos the CE marking would need to comply with that ce 1 Check risks related to health and safety of end users 2 Test sample of RE made available on the market 3 Investigate 4 Keep a register of complaints of non conforming RE and RE recalls and 5 Keep distributors informed of any such monitoring Note Not in EMCD and LVD Question Is complying with all the RE Harmonised Standards compara
4. Equipment Directive MRA Workshop March 2015 Japan Presented by VY 7u7 y Jan Coenraads secretary of R amp TTECA REDCA jan coenraads brynyago com ijian coenraads This presentation will cover Some upcoming changes in EU for equipment covered by the Radio Equipment Directive RED 2014 53 EU some specific aspects questions and answers For general aspects of the RED see also 2014 Workshop presentation 1 Directives EMC LVD RED 2014 30 EU 2014 35 EU amp 2014 53 EU 2 Blue Guide 2014 3 Guides for the Directives zzzz z to be developed PROGRESS 4 HS List in the OJEU 5 EU Commission amp R amp TTECA sites 8 Radio equipment related websites ECC EFIS ETSI CENELEC etc The specific product legislation for Telecom e LVD Electrical equipment designed for use within certain voltage limits 2006 95 EC 2014 35 EU e EMCD Electromagnetic Compatibility 2004 108 EC 20174 30 EU R amp TTE Directive 1999 5 EC Radio Equipment Directive 2014 53 EU EMCD and LVD never apply for Radio Equipment under RED when the product is placed on the market until it reaches the end user transferring products for testing or validating pre production units Is considered still in the stage of manufacture to all forms of supply including distance selling to newly manufactured used and second hand products imported from a thi
5. ble to have done the risk assessment Applying the HS is the basis but you should be able to understand what the risks of the RE are The HS may however not cover some aspects e g ageing of products specific use frequency ranges not covered The Commission indicated that a manufacturer should perform a risk assessment first and then apply the HS to demonstrate that the risks have been adequately addressed and mitigated Administrative non compliances are not considered to be a risk only technical ones Extra RED requirements not in EMCD amp LVD er I Software requirements Product registration Simplified DoC Information in user instruction Geographical information START 12 June 2018 gt Only for RE that have been identified for registration based on low compliance rate gt Registration includes providing elements of the technical documentation gt The Commission shall specify which RE categories are concerned and the elements of the technical documentation to be provided and the operational rules for registration and affixing the registration number on RE for the categories specified gt Each RE will be allocated a registration number that must be affixed to each RE of the type gt Manufacturers shall use the central system for registration provided by the Commission That system shall ensure appropriate control of access to information of confidential nature RED Instructi
6. hin each MS Therefore in the RED there is no need to include additional provisions such as prior notification 12 Broadcast Receivers and transmitters lt 9kHz are in the RED scope per 13 June 2016 move out of EMCD amp LVD There is a transition period until 13 June 2017 Those products can thus use either new EMCD in operation per 20 April 2016 or the RED After 13 June 2017 they can only apply the RED Equipment changing from LVD EMCD to RED 2 So for 2 months only 20 April 2016 13 June 2016 these products MUST use the NEW EMCD amp LVD and then move to the RED or stay in EMCD LVD until 13 6 2017 The EU Commission has requested the National authorities to apply a pragmatic approach during this period In general products during the transition period need to have a DOC that clearly indicate to which Directive they apply So do not indicate both Directives on your DOC This applies to Telecom Terminal equipment TTE all equipment after the Network Termination point not having a radio function Examples gt Office telephone exchanges gt Telephones gt Fax machines gt Routers gt In house PLC equipment etc Transition for Equipment changing from R amp TTED to LVD amp EMCD 2 On 13 June 2016 they automatically move to the New EMCD amp New LVD So these equipment MUST use the new EMCD and New LVD from 13 June 2016 onwards There is no tran
7. languages 2 A major advantage could be that when something needs to change in the DoC remember the RED says the DoC should be continuously updated you can easily do that on the website without having to change the paperwork in the product package The standard simplified text does not need to change in most cases Question Must mention Batch or Serial numbers of my product on the DoC Answer This identification is mandatory to acquire a link between the product and the documentation For some products it may be necessary to use batch or serial number to correctly identify the product This could be e g the case for explosives or certain medical implants But for most equipment under the RED the product name and model or type would normally be sufficient to link the documentation to the correct equipment Question What happens if a HS change and my product is still being put on the market Answer Check if re testing Is necessary change of state of the art Adapt Technical information Change DoC HS reference Ask help from NB if necessary Question Can RE manufactured in China choose an NB CAB in Japan Answer Yes a manufacturer Is totally free to choose the service of any appointed NB on the EU NANDO list including those outside the EU such as the possible 2 RED NB in Japan Question If New RED EMCD or LVD is operational new number do need to change the D
8. oC of my product Answer If apparatus is still entering the EU market then you must use the new number on the DoC so update the DoC but also check if reassessment is necessary DOC must be up to date when Individual product enters the market Note DoC Layout si TED Marking zes in future will change Appearances R amp TTED Harmonised standards applied for radio aspects no user restrictions no NB used RED Standard route Module A or module BC used R amp TTED Harmonised standards applied for radio aspects user restrictions NB not used R amp TTED Harmonised standards for radio aspects not applied or module B C applied for other aspects user restrictions NB used R amp TTED Harmonised standards for radio aspects not applied or 4 3521 module B C applied for other aspects no user restrictions NB used RED Module H used number is of NB 38 When Technical documentation is not complying and fails to present sufficient relevant data or means used to ensure compliance of RE with the essential requirements Market surveillance authorities may ask the manufacturer or the importer to have a test performed by a body acceptable to the market surveillance authority at the expense of the manufacturer or the importer within a specified period in order to verify compliance with the essential requirements Is R amp TTECA of interest to you REDCA in future REDE Most rapid acce
9. on manual RE must be accompanied by instructions and safety information in a language which can be easily understood by consumers and other end users as determined by the MS concerned Instructions shall include v Information on RE intended use v Where applicable a description of accessories and components including software which allow the RE to operate as intended Such instructions and safety information as well as any labelling shall be clear understandable and intelligible Only for transmitters Frequency band s in which the RE operates Maximum radio frequency power transmitted in the frequency band s in which the RE operates 27 Product information Manufacturers shall ensure that RE v bears a type batch or serial number or other element allowing its identification v contain their name registered trade name or registered trade mark and the postal address at which they can be contacted The address shall indicate a single point at which the manufacturer can be contacted The contact details shall be in a language easily understood by end users and market surveillance authorities Where the size or nature of the RE does not allow it the required information shall be provided on the packaging or ina document accompanying the radio equipment 28 Geographical area information The packaging shall v allow to identify the MS or the area within a MS where RE can be put into service
10. rd country when entering the EU market for the first time A product is made available on the EU market when supplied for distribution consumption or use as a commercial activity whether in return for payment or free of charge Each individual product must comply with the Directives at the moment of placing on the EU market measures from 13 June 2016 R amp TTED 1 1 RED transposed in MS 2 RED aiaiai in MS 1 Remaining MS R amp TTED R amp TTED DoC can be DoC can used be used Moment of placing an individual product on the market TRANSPOSITION PERIOD RED Timing of the RED 2014 53 EU MS shall adopt and publish by 12 June 2016 the national legislation necessary to comply with this RED They shall apply those Only R amp TTED DoC can be used V MS shall not impede the making available on the market or putting into service of RE which is in conformity with the relevant Union harmonisation legislation applicable before 13 June 2016 and which was placed on the market before 13 June 2017 TRA lt NSITIONAL PERIOD RED R amp TTED 13th JUNE mK 13th JUNE 2016 2017 R amp TTED Only DoC or RED nari ha DoC can used be used RED DoC RED is applicable from 13 June 2016 So before 13 6 2016 The RED shall not be used DOC making reference to the RED shall not be used e RED NB s shall
11. sition period However the Commission requests the national authorities to apply a pragmatic approach and accept the old DOC s to be used for a certain period may be until end of 20167 It does not matter what the Main function is 2014 53 EU EMCD LVD What changes when incorporate a wireless device gt The routes to compliance e g Module H gt Several administrative requirements gt Some technical requirements gt Test requirements harmonised standards One of the problems can be Emission limits for RED HS more severe different than for EMCD HS Where can I get guidance for this TR 102 070 Guide to ETSI TR 102 070 1 v1 2 4 2003 12 ETSI TR 102 070 2 v1 1 1 2002 11 z A ee the application of S harmonized standards to Electromagnetic compatibility Electromagnetic compatibility and Radi t Matt ERM and Radio spectrum Matters ERM 7 Guide to the ilicis of tiani pemi ara Guide to the application of harmonized Sadik to m u Iti ra d i O a n d multi radio and combined radio and non radio equipment multi radio and combined radio and non radio equipment 7 Part 1 ElectroMagnetic Compatibility Part 2 Effective use of the radio frequency spectrum CO m b i n ed ra d I O a n d n O n radio equipment e currently under consideration It is expected that R amp TTECA TGN O1 see www rtteca com the RED Guidelines Technical Guidance Note on the R amp TTE
12. ss to the constantly changing EU legislation regulation and EU Standards development Possibility to get rapid answer from fellow experts on specific R amp TTED RED technical questions gt 130 members Annual Fee 500 EURO Interested Go for information to www rtteca com or talk to me End of Presentation Thank you tor your attention Any QUESTIONS 41

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