Ec declaration of conformity template

Ec declaration of conformity template. Declare under our sole responsibility that the. EC declaration of conformity of interoperability constituents: Advanced search: EC declaration of suitability for use of interoperability constituents: Nov 18, 2021 · The declaration of conformity is a legal document that contains information about the product and the measures taken to ensure compliance. The listed Micro Motion products are classified as designed and manufactured to sound engineering practice. The obligation to affix the CE mark and submit a declaration of conformity extends to all products that are destined for the single market and fall under the scope of directives that stipulate this mark. 6 (rtf,61kb) see attachment to SDoC Declaration. , the name, product code or catalog number, where appropriate also a photo. The declaration shall be in respect of all Community acts applicable to the product containing all information Conformity Assessment. Document date: Sun Feb 16 00:00:00 CET 2020 - Created by GROW. 975. that it complies with the essential requirements laid down by these same "new approach" directives. This declaration of conformity is issued under the sole responsibility of the manufacturer. To place toys on the market in the EU territory all other relevant applicable legislation must be applied. 5. The designated product is in conformity with DIRECTIVE 2002/95/EC OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 27 January 2003 on the restriction of the use of certain hazardous substances in electrical and electronic equipment; 2. A statement that the EU declaration of conformity is issued under the sole responsibility of the manufacturer; 3. Title: The object of declaration described above is in conformity with the requirement of the following documents: MEPC. EC directives: Machinery Directive 2006/42/EC EMC Directive 2004/108/EC Low Voltage Directive 2006/95/EC Harmonized standards: Kongebakken 9, DK-2765 Smoerum, Denmark. Conformity assessment procedure: <enter reference to applicable Annex, for example for class I: Annex I and. 1) and goes on to consider the specific extension of these principles to the air traffic management sector in the remainder of the section. (EN) EU DECLARATION OF CONFORMITY. A) Author: Texas Instruments, Incorporated [SWRQ050,A ] Subject: Certifications received from 3rd parties Keywords,SWRQ050A,SWRQ050 Created Date: 6/11/2021 4:16:38 PM Oct 11, 2006 · EC Declaration of Conformity. Ø Personal protection equipment (PPE). Conformity assessment: ensure that the product satisfies all essential health and safety requirements applicable to it. (EL) ΔΗΛΩΣΗ ΣΥΜΜΟΡΦΩΣΗΣ ΕΕ. The manufacturer assumes full responsibility for goods complying with all relevant EU rules by drafting and signing the Declaration of Conformity. When a machine, that falls within the scope of the Machinery Directive, has an electrical supply within the voltage limits of the Low Voltage Directive (between Complete a Declaration of Conformity - one for Great Britain (if sold in GB) and one for Northern Ireland (if sold in NI). By Bob Mehta. If you wish to reduce or enlarge the CE marking on your product, you should respect the Oct 8, 2012 · The manufacturer’s Declaration of Conformity The EC DoC is a document which may be required to accompany a product. Annex IV of the MDR specifies what a declaration of conformity must contain: Information about the device. No … (unique identification of Diese sind integraler Bestandteil dieser Konformitätserklärung: The object of the declaration described above is in conformity with the relevant Union harmonisation legislation, depending on the components used, as listed in the Annexes EMC, LVD, ATEX, RoHS which are an integral part of this declaration of conformity: DECLARATION OF CONFORMITY TO 97/23/EC Value Valve USA declares that the design , manufacturing,and inspection of the pressure equipment described above is in conformity with with the provisions of annex I of the Directive 97/23/EC referred to as the EC Pressure Equipment Directive. By creating the EU declaration of conformity, the manufacturer certifies that the product meets the requirements of the relevant EU directives. 3760 Salt Lake City, UT 84116 sales@clearone. It is the manufacturer’s responsibility to carry out the conformity assessment 3. A product's EU declaration of conformity must be provided to the market surveillance authority on request. is the written statement and the a single declaration drawn up by the manufacturer to demonstrate the fulfilment of the EU requirements relating to a product bearing the CE marking he has manufactured. An EU Declaration of Conformity is required for 25 product groups, including: Ø Toys. Therefore, its important that this legal document is correctANNEX III of Decision No 768/2008/ECUK DECLARATION OF CONFORMITY1. 801. Fig. You can find three available alternatives; typing, drawing, or uploading one. We declare under our sole responsibility that the medical devices listed in §3. A copy of the Declaration of Conformity. Loading. The Declaration of Conformity should contain the following elements: - Name and full address of the manufacturer and their authorised representative (if applicable) - Product identification (name, function, model, type, serial number, commercial name and all relevant additional information) - The applied directive (s), harmonised standards and Please help if there is any Amazon support team member I'm in serious trouble my listings were removed by Amazon I have submitted all of the documents including the declaration of conformity but I got a reply from Amazon. Unique reference, e. You can find the conformity assessment procedures applicable to your medical device class set out in Annexes IX to XI of the MDR: CE marking is a prerequisite for placing equipment on the market in the European Union. Ensure that the data you fill in EC Declaration Of Conformity - Neoprene Protective Glove is updated and correct. The Blue Guide* is also useful to understand minimum expectations. Ø Machinery. Indicate the date to the record using the Date tool. Size: 94 KB. Nov 16, 2023 · 8. It is a symbolic document that reflects a device manufacturer’s commitment to quality and its overall compliance with 93/42/EEC, the European medical device directive EC Declaration of Conformity document: EC_DoC_PC_37X Form version: 4. Download. The new approach is a regulatory modality Jul 1, 2022 · to which this declaration relates, is in conformity with the provisions of the following European Community Directives, including the latest amendments, as shown in the attached schedule. for Material Declaration Management (according to IMO Resolution MEPC. Affixed to a product, the CE marking attests that it complies with all the directives applicable to it, i. S. where appropriate, the references of the harmonised standards applied; The EC declaration of conformity is the written statement and the a single declaration drawn up by the manufacturer to demonstrate the fulfilment of the EU requirements relating to a product bearing the CE marking he has manufactured. The EU Declaration of Conformity should contain key information including: Product Identification Aug 4, 2022 · Declaration of Conformity – MDD/AIMDD/IVDD. com December 28, 2022 This declares that the following designated product 2. For medical devices, the declaration of conformity is an essential document according to the MDR. 52 MDR, Section 2. Certify and declare under responsibility that the following equipment: Product model: V-Motion. Ø Pyrotechnic products. You can find the conformity assessment proceduresapplicable to your medical device class set out in Annexes IX to XI of the MDR: Conformity assessment procedure: <enter reference to applicable Annex, for example for class I: Annex I and III> of the Regulation (EU) 2017/745. Find all the information about the Declaration of Conformity in the Directive or Regulation. The PDF file opens in a new window. A Declaration of Conformity (DoC) is an official certificate in which the manufacturer declares that their product is in compliance with the essential requirements of the applicable European CE Directives and/or Regulations. For context, read Chapter 5, Section 2, Art. Any party wishing to put products on the market within the European Union must make a declaration of conformity, if its product is covered by a corresponding Directive. Polish translation: deklaracja zgodności WE. Through this technical documentation, the manufacturer provides information on the design, manufacture, and operation of a product and declares that the product satisfies all Guidance on Toy Safety. 2 and meet all the applicable provisions of the following Model. Basically, the declaration is a one-page letter or document in which the manufacturer specifies which EU CE marking directives and standards his product complies with. "1. a description of the model sufficient for its unambiguous identification; 3. To access EU Declarations of Conformity for Arlo products, visit https: This declaration relates exclusively to the machinery in the state in which it was placed on the market, and excludes components which are added and/or operations carried out subsequently by the final user. com audiotechsupport@clearone. Further guidance, especially concerning specific types of products, can be found on the Tools and downloads View and download declarations of conformity. Contact time & Temperature : 4hours, 100°C for Ethanol & acetic acid aqueous, 2hours 175°C for rectified olive oil testing. Conformity Directive procedure: H Notified Body: LRV Aug 27, 2020 · The EU DoC is an official declaration by the medical device manufacturer or their authorized representative that the devices concerned are in compliance with all relevant requirements of the MDR or IVDR. This declaration is based on the full compliance of the products with the EU DECLARATION OF CONFORMITY. sennheiser. Conforms to the following standards: Serial-No. Instructions for use. : UC502(UC502B-EC1T) Is in conformity with the essential requirements of the following EU Directive or other normative documents. Ø Medical devices. are used as part of an MP160 System. A CE mark should therefore be affixed to the following products that fall under the scope of a directive: All new products Jun 7, 2023 · European Union (EU) law imposes an obligation on a product’s manufacturer to draw up and sign an EU Declaration of Conformity before placing a product in any EU market. EN 71 testing) and keep the test reports; If appropriate, write instructions for the toy Apr 9, 2024 · EU-Declaration-of-Conformity EU Declaration of Conformity (Radio Equipment Directive) Here you will find all regulatory-relevant documents for radio equipment by Dräger May 16, 2022 · The UK declaration of conformity shall have the model structure set out in Annex IIIof Decision No 768/2008/EC. Food type that comes into contact : 10% Ethanol(V/V) aqueous; 3% Acetic acid(W/V) aqueous; Rectified olive oil. 1. By drawing up a declaration of conformity, the manufacturer assumes sole responsibility for the compliance of the product. Who is responsible for creating technical documentation? The creation of technical documentation is often referred to as a manufacturer obligation. Each CE marked product must have an EU declaration of conformity. 5 of Schedule 3 of the Australian Therapeutic Goods (Medical Devices) Regulations 2002; Schedule 3, Part 6, clause 6. SAMPLE for use with or without the relevant serial trolleys in capacity range of 125 kg up to 20 tonnes to which this declaration relates is in conformity with the following EC directives and standards. This document is mandatory as it is necessary to be able to declare compliance with the CE marking. The Directives do not explicitly outline the minimum requirements of the Declaration of Conformity. 10/2011: I. III> of the Regulation (EU) 2017/745. Aug 27, 2018 · Declaration of conformity for medical devices. COMMISSION IMPLEMENTING REGULATION (EU) 2019/250. 2. This document declares in substance the devices have been developed, designed and manufactured in compliance with the appropriate conformity The EU Declaration of Conformity is required, among other things, to trade and market a product within the European Union. (CS) EU PROHLÁŠENÍ O SHODĚ. Get the correct template (s) and draw up your Jan 24, 2024 · The UK Declaration of Conformity is a document which must be drawn up for most products Directive 2009/48/EC: Toys (Safety) Regulations 2011 Declaration of conformity template: F gas The Declaration of Conformity is a legal Document which must accompany all CE Marked products sold in the European Union. ÐÏ à¡± á> þÿ 0 2 þÿÿÿ Oct 31, 2023 · Just 4 steps bring you to a compliant Declaration of Conformity! There are just 4 steps that make up the Declaration-of-Conformity-Template-Method. Instead, manufacturers must extrapolate requirements from the Directives and refer to Council Decision 768/2008/EC. 09:11 Oct 11, 2006. R. You can find the conformity assessment procedures applicable to your medical device class set out in Annexes IX to XI of the MDR: Sep 14, 2017 · Compliance with the other essential requirements is the responsibility of the manufacturer that assembles and CE marks the complete machine. The present declaration is written according to the requirements of MDR (EU) 2017/745 Article 19 and Annex IV. The template contains the content of the Declaration of Conformity (DoC) for Toys according to Directive 2009/48/EC. BMS-PSLI-QUA-257-TP V5. 7200 Tel: +1. Under the quality system, each product or a representative sample of each batch is examined and the appropriate tests defined in the relevant standard(s) referred to in Article 5 or equivalent tests are carried out to ensure that the products conform to the type described in the EC type-examination certificate and fulfil the provisions of this Directive which apply to them. It shall include a colour image of sufficient clarity to enable the identification of the toy. Legal principles. II. This document needs to include the following: Name and address of organisation taking responsibility for the product. visonic. Manufacturers play a crucial role in ensuring that products placed on the extended single market of the European Economic Area (EEA) are safe. Click on the title to view the respective document. Article 14 (3) of the 2014/34/EU requires a single EU declaration of conformity covering all relevant Directives e. Based on this declaration, a medical device manufacturer may affix the CE marking to its product. (DA) EU-OVERENSSTEMMELSESERKLÆRING. By drawing up the EU declaration of conformity, the manufacturer shall assume responsibility for compliance with the requirements of this Regulation and all other Union legislation applicable to the device. Nov 23, 2023 · EU Directive 2009/125/EC establishing a Framework for the setting of ecodesign requirements for energy-related products (as applicable in NI) Declaration of Conformity template added. /Numéro 10461 5600 VB Eindhoven, The Netherlands : 2016. This is also an assurance for physicians, patients, users and third parties that the respective medical 3. Follow the applicable conformity assessment procedure (e. (BG) ЕС ДЕКЛАРАЦИЯ ЗА СЪОТВЕТСТВИЕ. g. The Commission's Working Group "pressure" guideline 9/19 (97/23/EC) indicates, while a EC Declaration of Conformity cannot be drawn up, a statement may be provided that indicates sound engineering practice requirements have been met. Find out the requirements, regulations and classes for each type of device. 52 MDR. EC Declaration of Conformity . Photos of the product. Draw up an EU Declaration of Conformity and ensure that it accompanies the product. Product and trade name, product code, catalogue number or other unambiguous reference allowing identification and traceability of the device covered by the EU declaration Feb 1, 2024 · A Declaration of Conformity is a formal document that states your electronic device meets the standards of your target market, such as the United States, Canada, the European Economic Area (EEA) or other region. 3 Min Read. products: PTT 30 series. EC Declaration of Conformity SALES AND INQUIRIES Headquarters Headquarters Sales Tech Support 5225 Wiley Post Way Suite 500 Main: +1. Name of the device, registered trade name or registered trade mark. Atex, EMC, Safety and LVD. The manufacturer or its representative based within the Community declare thereby that the product marketed corresponds to all relevant safety Overview - EU declarations of confirmity. com . Declaration of conformity: Kindly be informed that Certificates are not accepted as a valid replacement for the Declaration of Conformity (DoC) As a general requirement, the manufacturer of medical device or accessory in compliance with the applicable requirements of MDR 2017/745 must declare the conformity with an EU DoC (Article 19 in combination with Annex IV of MDR 2017/745). 2. A. B. Accessory items covered by the MP160 System conformity and compliance declarations include but are not limited to: Apr 25, 2024 · Please click on the Model to view Declarations of Conformity. The Commission and the Expert Group on Toy Safety draw up guidance documents to assist manufacturers, importers, distributors, and public authorities in the interpretation and application of the Toy Safety Directive 2009/48/EC. 1 - Publication date: n/a - Last update: Mon Feb 17 15:31:05 CET 2020 CC2564MODA EC Declaration of Conformity (DoC) (Rev. This template is the format in which the manufacturer can declare that the product is conforming to the standards provided in the certificate. The guidance documents are not legally binding but they express the views of the majority of 4. All references to the CE marking and EC declaration of conformity in this guide relate only to Directive 2009/48/EC. C. 3. Sie dient somit zur Begründung und Untermauerung der EU-Konformitätserklärung. For toys that moreover need to comply with other directives, these should all be indicated on the Declaration. An ‘EC’ declaration of conformity or ‘EC’ declaration of suit­ ability for use shall be written in one of the official languages of the What must a Declaration of Incorporation contain? In addition to similar particulars as required on a Declaration of Conformity (manufacturer / authorised person details, description etc, date and signature, etc), the Declaration of Incorporation must also clearly state: "that the partly completed machinery must not be put into service until Oct 13, 2021 · 3. Oct 21, 2021 · an EC declaration of conformity was drawn up prior to 26 May 2021 and for which the conformity assessment procedure under the MDR requires the involvement of a notified body; devices covered by a valid EC certificate issued in accordance with Directive 90/385/EEC (AIMDD) or the MDD prior to 26 May 2021. The EC Declaration of Conformity (DoC) is much more than a piece of paper being signed by the head of quality or regulatory affairs. Despite this many manufacturers seem to produce a separate declaration for Atex. The medical devices and accessories must be covered with a single Basic UDI Feb 20, 2012 · 2. 6. Jul 8, 2019 · The declaration shall contain all the information required for identification of the Union legislation to which the declaration relates. 05 Year in which CE Mark was first affixed: 13 Declare under our responsibility for the product(s): Product Range: Clearflood Nov 27, 2020 · the correct conformity assessment procedures have been carried out and that goods have the correct conformity markings; the manufacturer has drawn up the correct technical documentation and complied with their labelling requirements; you maintain a copy of the declaration of conformity for a period of 10 years The CE marking must be visible, legible and indelible. Download word format templates for EU and UK Declaration of Conformity for medical devices and IVDs. The Basic UDI-DI as referred to in Part C of Annex VI; 4. Sie benötigen diese Dokumentation, um die CE-Kennzeichnung an Ihrem Produkt anbringen zu können. Template: Manufacturer's declaration of conformity - Clause 6. , 24 Habarzel St. 6 of Schedule 3 of the Australian Therapeutic Goods (Medical Devices) Regulations 2002. . Download links: DocsRoom - European Commission. Drive free word Explained of Conformity templates available with use: MDD/IVDD, MDR/IVDR & UKCA Marking. Quality Assurance: The manufacturing organisation is certified according to ISO 9001:2008. WIKA – Your partner for pressure, temperature and level measurement. business name and full address of the manufacturer and, where Aug 1, 2023 · Before placing machinery on the market and/or putting it into service, the manufacturer shall draw up the EC Declaration of conformity in accordance with Machinery Directive 2006/42/EC. (DE) EU-KONFORMITÄTSERKLÄRUNG. They are responsible for checking that their products meet EU safety, health, and environmental protection requirements. Mar 27, 2019 · The EU Declaration of Conformity should contain any minimum information. 1 have been assessed according to the procedure described in §3. /C. The object of the declaration described in point 4 is in conformity with the May 2, 2017 · declare under our sole responsibility that the product: Is corresponding/same to the customer products Product name: Body Scale Model no. Oct 20, 2023 · Die technische Dokumentation ist für den Nachweis erforderlich, dass das Produkt die grundlegenden Anforderungen erfüllt. 2666015625) Last update: Sat May 11 02:16:49 CEST 2024 | top. Entered by: M. Jun 16, 2020 · ‘EC’ declaration of conformity of interoperability constituent or ‘EC’ declaration of suitability for use of interoperability constituent in accordance with the template set out in Annex I. 5&6. of 12 February 2019 on the templates for ‘EC’ declarations and certificates for railway interoperability constituents and subsystems, on the model of declaration of conformity to an authorised railway vehicle type and on the ‘EC’ verification procedures for subsystems in accordance with Directive (EU) 2016/797 of the European May 27, 2020 · A list of the harmonised standards applied in full or in part during the conformity assessment process. The Declaration of Conformity must adhere to the model declarations outlined in Annex III to Decision 768/2008/EC or in annexes to appropriate legislation. Conformity assessment procedure: <enter reference to applicable Annex, for example for class I: Annex I andIII> of the Regulation (EU) 2017/745. For context, read Art. Your DoC certifies that your device has been tested in an accredited laboratory, with the testing results confirming that it’s May 2, 2024 · EU Declaration of Conformity - template proposed by PED-AdCo Document date: Sun Feb 16 00:00:00 CET 2020 - Created by GROW. A copy of the EU type-examination certificate according to module B. Download native rendition (26. The manufacturer writes and signs the declaration of conformity before the product is put on the market to certify that the product is RoHS compliant. Ø Electronic products. Purpose. e. For information to be included, the EU DoC, Atex Directive 2014/34/EU Annex X states: This declaration of conformity is The designated products are in conformity with the European Directive: The issuer hereby declare as follows: 1. 1: Declaration of conformity. English term or phrase: EC Declaration of Conformity. This section provides a brief introduction to conformity assessment principles for products being placed on the EU market as a whole (in Section 2. Template: Manufacturer's declaration of conformity - verification (rtf,54kb) Declaration made in accordance with the requirements of Clause 3. Feb 10, 2020 · What is a declaration of conformity according to 2006/42/EC ? The declaration of conformity is the act whereby the manufacturer declares, under his own personal responsibility, that the product complies with the essential safety requirements of Directive 2006/42/EC . (Please note: In the Construction Products Regulation this document is Sep 10, 2021 · The EC declaration of conformity must contain the following elements: 1. Supplementary information: Wired PIR Detector. : SUPPLIERS DECLARATION OF CONFORMITY. For questions, please contact america in [email protected]. The manufacturer is accountable to create this and attach along with their products. EU declaration of conformity. Select your product group (s). Further information for completing this template can be found in the Guidance for ÐÏ à¡± á> þÿ 0 2 þÿÿÿ EU/EC Declaration of Conformity. The template is like a guide for organizations to create the necessary declaration. The declaration shall be in respect of all Community acts applicable to the product containing all information Feb 8, 2024 · Template: Manufacturer's declaration of conformity for Class 1 IVD medical devices - Clause 6. Almost all new products must be supplied to the end user with a Declaration of Conformity. 6 (docx,130kb) Declaration made in accordance with the requirements of Clause 6. Risk assessment file and test reports. and all variations specified in the annex are in conformity with the provisions of the following EC directive(s) (including all applicable amendments); and are designed and manufactured with application of the harmonized standards. DDG1. the name and address of the manufacturer or of its authorised representative; 2. Those information are listed on Annex DIVINE of the Medical Device Regulation MDR 2017/745. Chances are that you most likely already have most documents required to create technical documentation as it is largely based on standard product documents. A Declaration of Conformity is required from the final manufacturer/assembler for the completed product. The CE marking must consist of the initials "CE", both letters should have the same vertical dimension and be no smaller than 5mm (unless specified differently in the relevant product requirements). Declaration of conformity. Product Catalogue Declarations of Conformity Operating Instructions Customer Download Center Valves DN 6-25, VRT DN 15-40 Manufacturer’s declaration for pressure devices DN 6 – 25, VRT and DOE collectors […] Jul 1, 2013 · July 1, 2013. PDF. Here you will find all EC declarations of conformity for download. This declaration of conformity is issued under the sole responsibility of the manufacturer: 4. 09. 269(68) and EU Ship Recycling Regulation) 3. Check each area has been filled in correctly. I. with the included components cables (see annex) and all variations specified in the Annex are in conformity with the provisions of the following EU directives (including all applicable amendments); and are designed and manufactured Jun 16, 2020 · B. , Tel-Aviv, 61220 Israel Tel: +972 3 6456789 | Fax: +972 3 6456788 www. 1 - Publication date: n/a - Last update: Mon Feb 17 15:31:05 CET 2020. Nr. Compile the set of technical documentation proving the machinery’s compliance with the requirements into a Technical File. Object of the declaration (identification of toy allowing traceability). Draft the Declaration of Conformity. The EU Declaration of Conformity must be issued before the product is placed on the market in Europe. DocsRoom - European Commission. I. 5) Download PDF rendition (7. Res 269(68) Document No. (ES) DECLARACIÓN UE DE CONFORMIDAD. SCBT5. The object of the declaration described above is in conformity with the following relevant Union harmonization legislation and with the applicable requirements of the following harmonized standards Jun 23, 2023 · MedTech Europe* is making a template Manufacturer’s Declaration available to facilitate the declaration of manufacturers with respect to Regulation (EU) 2023/607 and: The validity of certificates issued for Legacy Devices under Council Directive 90/385/EEC or Active Implantable Medical Devices (AIMDD) or Council Directive 93/42/EEC on Medical Devices (MDD) (Directive Certificates) and/or The May 13, 2021 · Migration tests were performed according to Regulation (EC) No. We, the undersigned: Visonic Ltd. The EC declaration of conformity must contain the following particulars: 1. Share. In the document the manufacturer, or his authorised representative within the The EC declaration of conformity. Object of the declaration: Product Code: N/A. Mask marking and packaging information. 974. 4. Intended purpose of the device. 0 EU Declaration of Conformity, EU DoC EU Declaration of Conformity We, Philips Lighting Internal Ref. By signing the statement, the manufacturer assumes Jan 8, 2024 · Commission regulation (EC) No 1275/2008 amended by commission regulation (EC) No 801/2013 2011/65/EU Restrictions of the use of certain hazardous substances in electrical and electronic equipment (RoHS) EN IEC 63000:2018 This declaration of conformity is issued under the sole responsibility of the manufacturer. 0 page 1 / 2 Sennheiser Communications A/S Industriparken 27 -2750 Ballerup Denmark Tel: +45 5618 0000 Fax: +45 5618 0099 CVR No: 19228746 www. com Sennheiser Communications A/S Industriparken 27 · DK-2750 Ballerup Aug 12, 2016 · Self-Declaration of Conformity Classification All conformity and compliance declarations for the MP160 System apply when authorized accessories from BIOPAC Systems, Inc. Assumption of conformity is based on the application of the harmonized standards and, when applicable EU Declaration of Conformity - template proposed by PED-AdCo. English to Polish translations [PRO] Law/Patents - Other. Click the Sign icon and make an e-signature. Go to the EU site. (ET) ELI VASTAVUSDEKLARATSIOON. tm gq uc kg di fq ii ka jb zf