Declaration of conformity usa. Philips Solid-State Lighting Solutions .

Dec 27, 2021 · Declaration of Conformity Ref #: NU202167970 Rev #: 0 Manufacturer: Intel Corporation: Attn: Corp Quality 2200 Mission College Blvd, Santa Clara, CA 95054-1549, USA EU Single Place of Contact: Att. By drawing up and signing the EU Declaration of Conformity, the manufacturer (or, if applicable Declaration of Conformity. A Declaration of Conformity (DoC) is a legally binding document, in which the manufacturer asserts they have met the minimum requirements of the applicable legislation. This declaration of conformity is issued under the sole responsibility of the manufacturer who declares that the above- described radio equipment is in conformity with the following relevant Union harmonization legislations: Radio Equipment Directive 2014/53/EU (RED Supplier’s Declaration of Conformity (SDoC) Equipment approved using SDoC is required to be tested, however, it is not necessary to use an FCC-recognized accredited testing laboratory. In contrast to a CoC, a DoC is often used for non-automotive products, such as electronics, machinery, or other types of equipment. When product compliance with the respective regulatory product requirements has been confirmed, the FCC marking may be affixed to the product. I. We, Sound Devices LLC, declare under our sole responsibility that the product: Product Name: A20-RX Model Number: DDX1010 Description: Digital Wireless Microphone Receiver is in conformity with the The CE Declarations of Conformity provide confirmation of compliance of Thermo Fisher products to the European Union Directives. (SDoC) (2) A TCB may certify this equipment Update on SDoC - USA. USA IN&MOTION USA Contact : +1 (917) 403-3163 Monday to Friday, Aug 4, 2022 · This is a legally binding document, in which the manufacturer asserts that they have met the minimum requirements of the applicable legislation. Select an area and learn more about our wide range of products and applications for weighing, measuring and analyzing. RM310EC. Issued by Manufacturer Hoffman Enclosures, Inc. The Directives are legal documents (laws) issued on the authority of the Council of the EU and adopted by all member countries. US (FCC) – SUPPLIER’S DECLARATION OF CONFORMITY (SDoC) PROCEDURES ARE NOW IN EFFECT. For more than 45 years, the Somfy group has been improving living conditions using automation, by designing and Europe. 9. Except as otherwise stated in a specific standard, section 14 (a) of the CPSA, as codified in 16 CFR part 1110, requires domestic manufacturers and importers of certain general-use products (i. mersen. Earl Bakkenstraat 10 6422 PJ Heerlen The Netherlands Physio-Control declares that the CE marked product Product Name: LIFEPAK® 15 Monitor/Defibrillator Part Number(s): V15-2-XXXXXX ZV15-2-XXXXXX Where X represents any numeric digit Sep 14, 2017 · Compliance with the other essential requirements is the responsibility of the manufacturer that assembles and CE marks the complete machine. Siemens Healthcare Diagnostics Inc. This document needs to include the following: Name and address of organisation taking responsibility for the product. The following standards were applied: EMC EN 300 386 V1. A CE mark should therefore be affixed to the following products that fall under the scope of a directive: All new products CE marking. Ø Electronic products. 3M ESPE Dental Products Division 3M Center, Bldg 260-2A-11 St. Environment EC-Declaration-of-Conformity Here you can find the latest REACH and RoHS Declarations relating to ZF products. , non-children’s products) that are subject to a consumer product safety rules, or a similar rule, ban, standard Four Steps to Your Product’s CE Marking. c. Burlington, MA 01803, USA: Year in which CE Mark was first affixed: EC-Declaration-of-Conformity View the ZF product catalogue and download our switch and sensor range overviews to help you select the most suitable product for your application. sps. Ø Pyrotechnic products. Jun 13, 2023 · Create a table with two columns in a document or spreadsheet. Supplier’s Declaration of Conformity (SDoC) is an FCC equipment authorization procedure that requires the party responsible for compliance to ensure that the equipment complies with the appropriate technical standards. General Certificate of Conformity. com (this declaration is downloadable), USA SRN: US-MF-000013394 Declaration of Conformity Validity ISO 13485 #314505 MP2016 Expiry Date: 2024-11-07 Welch Allyn Limited, Navan Business Park, Dublin Road, Navan, Co. An overview of the CE Mark requirements for a Declaration of Conformity for machines, machinery and equipment that are to be sold in Europe. com www. Norwood, Massachusetts, USA Page 2 of 2 DMS 33-21-02 A Rev. UTAH 425 East 400 North Gunnison, UT 84634 Fort Mill, SC 29707 USA www. The ‘EU Declaration of Conformity’ (which is the most common term used in CE marking) is a document confirming that the product is placed in the Address: 425 Rue de Goa – Le Cargo B6 – 06600 Antibes Country: France. The undersigned hereby declares that the above reference product(s) to which this declaration relates is in conformity with the provisions of: Lot 3 (EU) No 617/2013 implementing measure of the Ecodesign Directive 2009/125/EC. FDA’s S Jan 24, 2024 · Conformity assessment. Article 14 (3) of the 2014/34/EU requires a single EU declaration of conformity covering all relevant Directives e. Theresa Glenna, Senior Project Manager, Global Market Access, discusses how the change to the EAC Declaration of Conformity Procedure, as of January 1, 2021, impacts companies. An EU Declaration of Conformity is required for 25 product groups, including: Ø Toys. 3D Files for Printing. Example: DIRECTIVE 2014/28/EU - explosives for civil uses. As a manufacturer, you must carry out a risk analysis and ensure that your products comply with certain rules before placing them on the EU market. As part of the CE Mark­ing process and the cor­re­spond­ing con­for­mi­ty assess­ment pro­ce­dure, man­u­fac­tur­ers must draw up a Dec­la­ra­tion of Con­for­mi­ty. In the EU, there are three officially (legally) recognized European Standardization Organizations (ESOs). Retail Scales. Paste your data into the list box on the left. The FCC mark adjacent to CE mark on an SMPS made in China and sold in India. In this page it is possible to download the EU Declaration of Conformity in accordance with the new Regulation (EU) 2016/425 on Personal Protective Equipment, in force since 21 April 2018. Enclosure Models Declaration of Conformity CEDec. It’s mandatory for most electronic devices sold in the United States, with devices requiring either certification from the FCC or self-declaration (Declaration of Conformity, or DoC) depending on their type. For example, CE Marking to the EU MDR or UKCA Marking to the UK Medical Devices Regulation 2022. DOWNLOAD - Sunglasses (PDF 2,8 MB) DOWNLOAD - Optical frames (PDF 0,5 MB) DOWNLOAD - ELLE readers (PDF 0,2 MB) Jun 14, 2024 · SLS 300 EC Declaration of Conformity. com for assistance. To which this declaration relates, are in conformity with the test requirements of the following standards: BS1363-2:2016+A1:2018. 1. Atex, EMC, Safety and LVD. Download here the declaration of conformity of the In&box and of the back protector. Paul, MN 55144 USA Annex Il, Clause 3 of Council Directive 93/42/EEC concerning Medical Devices. Note that the FCC Fort Mill, SC 29707 USA www. EN 300 328 V2. 374 MERRIMAC STREET — NEWBURYPORT, MA 01950 T 978 462 6662 — F 978 462 0181 — info. USA Company identification: EIN 47-2316603 European VAT number: DE318553720. Michigan City. Copy/paste in the left column the number of the article and in the right column the text which contains “declaration of conformity”. In sim­ple terms, the Dec­la­ra­tion of Con­for­mi­ty is the manufacturer’s for­mal dec­la­ra­tion that the devices The requirements for the Declaration of Conformity and the Certificate of Conformity differ, and product category usually determines which scheme a company must follow. Shipping from the USA to EGYPT - GOEIC must approve shipment to issue the mandatory Certificate of Inspection for exports of Regulated Products to Egypt. Step 2: We carry out the conformity evaluation procedure and all required audits on your behalf. Need Help? Call: . Meath, C15 AW22 : Ireland SRN: IE-AR-000000768 Object of the declaratio n . com DECLARATION OF CONFORMITY Page 4 of11 Revision Date 29-May-2019 Honeywell Internal 425388-0406 CABLE, USB A MALE TO USB 427508-0630 CBL ASSY, MINI DN6 M/F 427518-0913 CBL ASSY, D9 M/F 1:1 ST 50101274-001 Cable Black Coiled 50101275-001 Cable DUAL Ended Male An (EC/EU) Declaration of Conformity is a requirement for CE marking, and it serves as a signed declaration that a product complies with the relevant EU directives, regulations and/or standards, declaring its safety, performance, and conformity to essential requirements. com Contacts. Shipping from the USA to ETHIOPIA - Certificate of Conformity is mandatory. , 374 Merrimac Street, Newburyport, MA 01950-1998, Website ep-us. Template: Manufacturer's declaration of conformity - Clause 6. g. among those listed below: name and full business address of the manufacturing company or of the Authorized Representative. For more information about bringing your CE-certified product to the United States, or to learn more about any aspect of electronic device testing and Feb 15, 2019 · United States. This document demonstrates the fulfillment of the essential health and safety requirements applicable to the device with CE marking. 1-855-253-6686. This white paper gives you a thorough understanding of the key elements of the Low Voltage Directive and the Machinery Directive. If a DoC is required in a country, specifically in the European Union, the DoC confirms that a Supplier’s Declaration of Conformity (47 CFR Section 2. Supplier's Declaration of Conformity (SDoC) signifies that the This Declaration of Conformity is issued under the sole responsibility of the manufacturer. product serial number, model, or type identification. A Declaration of Conformity (DoC) is a required self-certifying document created by the medical device manufacturer to state that a device or a series of devices complies with the conformity requirements of a particular country’s regulations. Eaton 9PX. TEMPE 1236 West Southern Ave, Suite 101 Tempe, AZ 85282. Service. Fax: +1. TruScan G3 EU. Nachtigall, Technical Leader – Product Compliance Engineering. The unit covered by this declaration is in conformity with EU EMC Directive, 2014/30/EU (26 February 2014). 4499 Harmonized Standards (cited in the OJEU) and Presumption of Conformity. Corp Quality, Intel Deutschland GmbH, Am Campeon 10-12, Neubiberg, 85579 – Germany UK Single Place of Contact: Jan 12, 2021 · 01. Below we provide the medical device & IVD Declaration of Conformity requirements in Europe, the United A Declaration of Conformity (DoC) is a formal statement issued by a manufacturer or an authorized representative asserting that a product complies with all relevant regulations, standards, and directives required for it to be sold within a particular market or region. SLS 300 Water Jet Cabinet Customer Documentation. 2. We recommend that manufacturers have their UK Declaration of Conformity and their EU Declaration of Conformity in separate documents. Manufacturers of systems/procedure packs and custom-made devices must also draw up statements. O. Ø Personal protection equipment (PPE). declare at our sole responsibility, that these devices are designed and constructed according to . B. 410. Lab Analytical Instruments. 1 The responsible In the United States, several globally relevant approaches to conformity assessment are used in order to increase user confidence in products, processes, systems, or personnel. Assumption of conformity is based on the application of the harmonized standards and, when applicable or required, a The EU Declaration of Conformity (DoC) is a legal document, wherein a manufacturer formally declares the compliance of a particular product that falls within the scope of CE marking, with the essential health and safety requirements of the relevant product safety directives. U. A UKCA Self-Declaration of Conformity or a Declaration issued after a conformity assessment of a certifying body have exactly the same format and only differ by point 4. Other. 800 Independence Avenue, SW. Almost all new products must be supplied to the end user with a Declaration of Conformity. complies with the provisions of Union harmonization legislation: 2014/35/EU : LVD – Low Declaration of Conformity . These approaches include: 1st Party Conformity Assessment: Performed by the person or organization that provides the object, such as the manufacturer or supplier. Through this technical documentation, the manufacturer provides information on the design, manufacture, and operation of a product and declares that the product satisfies all II 3 G Ex ec IIC T4 Gc Type Examination Certificate No. Philips Solid-State Lighting Solutions . EPD TruDose G TEL. Specification for 13A switched and unswitched socket outlets Part 1: General requirements. [3] : 58 It is not a quality indicator or a certification mark. com Page 1 of 2 ep. Mar 2, 2023 · The UK Declaration of Conformity is a document that must be drawn up for most products lawfully bearing a UKCA marking before they are placed on the market. An identification of an alternative MERSEN USA EP Corp. USA. 6 (rtf,61kb) Dec­la­ra­tion of Conformity. Copy/paste all other hits to the table. RM310EC Declaration of Incorporation. 2011/65/EU RoHS Directive. Supplier’s Declaration of Conformity (SDoC) is a procedure that requires the party responsible for compliance ensure that the equipment complies with the appropriate technical standards. SLS 300 Software Downloads. ASCA's goals are to: Streamline Jul 3, 2024 · ensure conformity with all relevant EU-wide requirements; determine whether you can assess your product by yourself or if you have to involve a notified body; put together a technical dossier documenting conformity: find out about technical documentation; draft and sign an EU declaration of conformity Jul 15, 2023 · Contact. [4] . 3. com DECLARATION OF CONFORMITY We Mersen USA EP Corp. 316. Apr 27, 2022 · The authority additionally emphasizes that for Class B, Class C, and Class D medical devices, declaration of conformity to either of the following QMS standards is mandatory: ISO 13485, US FDA Quality System Regulations, and Japan MHLW Ordinance 169. Single Registration Number (SRN) Manufacturer: US-MF-000018066. 346 - Description of Testing Facilities • Responsible party shall retain a description of the testing facilities used • Required description to be given by the Administrative Declaration of Conformity . Producing a Declaration is one of the integral tasks involved in CE marking a product or machine. EU EMC Directive An identification, for each consensus standard, of any way (s) in which the standard may have been adapted for application to the device under review (e. Even if you subcontract the design or production of your DECLARATION OF CONFORMITY. A Certificate of Conformity on the other hand is issued by a third party. 6. 3 Burlington Woods Drive . com Urgent export compliance issues: exportalert@fortinet. Maximum number of part numbers that can be processed at 1 time: 200. S. Despite this many manufacturers seem to produce a separate declaration for Atex. 1080 US Highway 202 South Branchburg, NJ 08876 USA. EN 62623:2013. The EU Declaration of Conformity is a part of the conformity assessment procedure in accordance with the EU product legislation. In the document you as the manufacturer, or your Somfy operates in 58 countries and is the world leader in automatic controls for openings and closures in homes and buildings. 4000 . e. EN50130-4:1995 + A1:1998 A2: 2003 EC Declaration Of Conformity Physio-Control, Inc. hhs. IN 46361. We herewith declare that the above-mentioned product(s) meet the provisions of the Council Directive 98/79/EC for in vitro diagnostic medical devices. In the event that the unit covered by this declaration does not have its own enclosure, the unit does not meet the definition of “apparatus” or “fixed installation” as defined by the Guide for the EMC Questions regarding Fortinet’s product regulatory compliance such as requesting Declaration of Conformity, please contact ProdRegCompliance@fortinet. honeywellaidc. For information to be included, the EU DoC, Atex Directive 2014/34/EU Annex X states: This declaration of conformity is Supplier's Declaration of Conformity is the procedure by which a first party or supplier conveys assurance that the object of conformity fulfills specified requirements. Department E-Mail: tradecompliance@fortinet. com Sparks, Maryland 21152, USA . The Declaration of Conformity must be issued by the “manufacturer” or their to which this declaration relates, are in conformity with the following Directives and Standards: Directive 89/336/EEC, The EMC Directive . Document Control Number: 1756-CT209A-EN-E. Grafenberger Allee 277-287 40237 Düsseldorf, Eingang C Germany. EC DECLARATION OF CONFORMITY 3M Center, Bldg 260-2A-11 St. A EU Declaration of Conformity (also called a CE Certificate, EC Declaration of Conformity, or CE Declaration of Conformity) is the document confirming that the product complies with the applicable CE marking directives or regulations. In most cases, when a product is covered by several product safety directives, only a single DoC needs to be drawn up. The presence of the logo (from French, "conformité européenne" meaning "European conformity") [2] on commercial products indicates that the manufacturer or importer affirms the goods' conformity with European health, safety, and environmental protection standards. The Declaration of Conformity (DoC) in the User's Guides and/or Quick Setup Guides may be an earlier version. ECG Multifunction Electrode Adapter Find environmental and regulatory information and resources for Apple products and services. Ascensia Diabetes Care Holdings AG Peter Merian-Strasse 90 4052 Basel, Switzerland Tel: +41 58 272 77 00 Sep 19, 2023 · The testing is accompanied by a complete declaration of conformity and an ASCA Summary Test Report, and The standard and test methods are within the testing laboratory's scope of ASCA Federal Communications Commission Office of Engineering and Technology Laboratory Division. Department of Transportation. However, as minimum the testing laboratory used is required to maintain a record of the measurement facilities as specified in Section 2. PXS10 X-ray Source. Ø Machinery. 0 . 2021. Ø Medical devices. 12. Issuing a DoC is mandatory when manufacturing or importing products that require CE marking. Overview The 'FCC Declaration of Conformity' for personal computers that are assembled from components that have been separately authorized. With a declaration of conformity, you demonstrate that your product complies with all valid regulations, such as health and Jan 30, 2024 · We’ve also discussed the typical process for completing CE testing and achieving compliance for your electronic device, from testing to a Declaration of Conformity (DoC) or certification. INTRODUCTION. Meath, C15 AW22 Ireland SRN: IE-AR-000000768 Object of the declaration Laryngoscopes Apr 9, 2014 · Declaration of Conformity . 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. EPD TruDose BG TEL. Declare under our sole responsibility that the following product, which is defined as a „GPS Tracker“ Which is manufactured and sold by our company as the product model TRKM015: Meet the The EU Declaration of Conformity is a document, in which the manufacturer declares that the product conforms to the requirements. types within the range on page 2. Federal Aviation Administration. gov. Hit Export Spreadsheet button to create XLS file containing links to relevant Declarations of Conformity. Effective February 15, 2019. Title. This article explores the significance, requirements, and examples of DoCs in the United States and the European Union. nby@mersen. 906); this procedure is aimed at products that unintentionally send & receive signals. These produce “harmonized EN (European Norm) standards”. UL 22 ATEX 2819X Signed for and on behalf of the above named manufacturer: Place and date of issue: Name, function: Signature: Milwaukee, WI USA 03-Oct-2022 Daniel L. The EU Declaration of Conformity should contain key information including: Product Identification The responsible party for the Supplier's Declaration of Conformity must be located within the United States. V. 948 and a record of (b) If the device that is subject to a Supplier's Declaration of Conformity is designed to operate in conjunction with other equipment, the characteristics of which can affect compliance of such device with part 68 rules and/or with technical criteria published by the Administrative Council for Terminal Attachments, then the Model Number(s) of Sep 19, 2023 · The voluntary ASCA Program is an accreditation scheme that capitalizes upon the increasingly prominent role that standards play in regulatory science and practice. This procedure is called a conformity assessment and it is carried out during both the design and production phase. The Declaration of Conformity is a legal Document which must accompany all CE Marked products sold in the European Union. Paul, Minnesota 55144 USA 3M ESPE Dental Products Division 211 McGaw Avenue Irvine, California 92714 USA Product Family: Aug 2, 2023 · CORE™ Digital Attachment Declaration of Conformity (DOC003) DUO™ ECG + Digital Stethoscope Declaration of Conformity (DOC002) Eko Analysis Software (EAS) Declaration of Conformity (DOC Mar 12, 2020 · The Declaration of Conformity is mandatory for any product that falls within the scope of the CE marking legislation. The manufacturer draws up and signs the declaration and states that the product fulfils An official website of the United States government Here’s how you know . Template: Manufacturer's declaration of conformity - verification (rtf,54kb) Declaration made in accordance with the requirements of Clause 3. EN61000-6-3:2007: -- Electromagnetic Compatibility – Part 6-3: Generic standards - Emission standard for residential, commercial, and light-industrial environments. A. (219)879-8868. Tel: +1. provided that it is installed, maintained and used in the application intended for, with respect to the relevant manufacturer’s instructions, installation standards and “good engineering practices”. declare under our sole responsibility that our Series DCGII Digital Pressure Gauge to which this declaration relates are in conformity with the following EC Directives and harmonized standards: Directive 2004/108/EC (EMC) EN 61326-1 (2006) Electrical Equipment for must issue a Declaration of Conformity (DoC) in order to sell their products in the EU. 8200 Market Boulevard Chanhassen, MN 55317-9685 USA. In accordance with EU Regulation 2017/746 of the European Parliament and of the Council of 5 April 2017 onin vitrodiagnostic medical devices. The Enforcement Bureau (EB) of the Federal Communications Commission (FCC or Commission) has issued this Advisory to remind any entity marketing radio frequency (RF) devices (marketers) that the devices may be Mar 19, 2024 · A declaration of conformity (DoC) is a vital document certifying that a product complies with legal standards, ensuring it is safe and fully operational for consumers. The Manufacturer retains all supporting documentation. Manufacturer’s Name: Sound Devices, LLC Manufacturer’s Address: E7556 State Road 23 and 33 Reedsburg, WI 53959 USA. All US machinery needs CE Marking before it EU Declaration of Conformity. Copy the column of Molex part numbers from your spreadsheet*. com DECLARATION OF CONFORMITY Page 2 of 3 Revision Date: 24-Jan-2024 SCANNERS: Voyager 1602g family Xenon 190xh family Granit 1280i family Stratos 2400 family Voyager 120xg family Xenon 1950h family Granit191xi family Stratos 2700 family conformity with Directive 2011/65/EU on the restriction of the use of certain hazardous substances in electrical and electronic equipment. 2 Wideband transmission systems; Data transmission equipment operating in the 2,4 GHz band Harmonised The Declaration of Conformity is a legal document in which the manufacturer or authorised representative signs to state that all CE Marked products sold in the European Union, meets all of the requirements of the applicable EU directives and regulations. It is a key component of regulatory compliance, particularly within the Oct 20, 2023 · An EU declaration of conformity (DoC) is a mandatory document that you as a manufacturer or your authorised representative need to sign to declare that your products comply with the EU requirements. x 3. The place and date of the declaration. The identity, position, and signature of the person signing the document. SDoC Section 68. Jan 5, 2020 · FCC Authorization Requirements (1) TTE does not require the use of an accredited lab. SLS 300 Customer Information Bulletins. NetDose CE. Automated Reactors. The responsible party, who must be located in the United States, is not required to file an equipment authorization application with the Commission or a TCB. Step 1: Our employees determine which directive are applicable to your product. We, Instruments. Manufacturer:Roche Molecular Systems, Inc. Read the text carefully. 2100 Hoffman Way, Anoka, Minnesota 55303-1745, U. 1:2012 EN 55032:2015/A11:2020 EN 55035:2017/A11:2020 EN 61000-3-3:2013+A1:2019 EN 61000-3-3:2013+A2:2021 EN IEC 61000-3-2:2019+A1:2020 CISPR 32:2015 Declaration of Conformity (DoC) A Declaration of Conformity, on the other hand, is a document that is issued by the manufacturer of a product to declare that the product meets the necessary regulatory requirements. The document should also contain references to the applicable international standards. P. Expand Tree Branch. A Declaration of Conformity is required from the final manufacturer/assembler for the completed product. Jan 24, 2024 · For general regulatory information, please contact the Division of Industry and Consumer Education (DICE) by phone at: (800) 638-2041 or (301) 796-7100 or by email at: DICE@fda. The subset of harmonized standards that are cited in the Official Journal of the European Union (OJEU) are Feb 28, 2024 · FCC Part 15 ensures that devices don’t interfere with wireless communications. 11811 Willows Road NE Redmond, WA 98052 USA Medtronic B. By signing the DoC you take full responsibility for your product's compliance with the applicable EU law. Get Lenovo's EU Declarations of Conformity for products and learn about our compliance with European Union regulations. This document is a crucial component of the CE marking process Shipping from the USA to ECUADOR - Government securing imports, facilitating exports, implementing importing standards. It offers a range of motorized solutions and control points and is a key player in smart home systems. Example of a declaration of conformity generated through the CE-Marking assistant web application. Washington, DC 20591 (866) TELL-FAA | (866) 835-5322 USA SRN: US-MF-000013394 Declaration of Conformity Validity ISO 13485 #35916 Expiry Date 2025-06-01 : Welch Allyn Limited, Navan Business Park, Dublin Road, Navan, Co. the fundamental safety and health requirements. Required Elements for a Declaration of Conformity to a Recognized Standard . 2. Legal principles. METTLER TOLEDO is a global provider of precision instruments and services for professional use. If you are unable to find your document, please email us at compliance@lenovo. Oct 5, 2023 · A Declaration of Conformity (DoC) is a document issued by the importer or manufacturer ‘placing the product on the market’. The EN and ISO standards utilized (recommended). 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. CALIFORNIA 3 Morgan Irvine, CA 92618. to which this declaration relates, is in conformity with the provisions of the European Union Directives, including the latest amendments, as shown in the attached schedule. Attachment 1 Instructions: 1. 5 of Schedule 3 of the Australian Therapeutic Goods (Medical Devices) Regulations 2002; Schedule 3, Part 6, clause 6. Content current as of: 08/04/2022. For the latest version please refer to our web site. Laboratory Division. Please find below EU and UK Declaration of Conformity templates available for The EU Declaration of Conformity is required, among other things, to trade and market a product within the European Union. honeywell. This is to declare that the products listed below including their required accessories have been manufactured according to the following EU directives: t Directive 2014/53/EU (RED)The radio equipment directive 2014/53/EU (RED) establishes a regulatory framework for placing r. fn ow hh tp kk ey ji jm ey jo