DOC模板 - EU Declaration of Conformity 2015-06-15

EC Declaration of ConformityBT/CE-04-2014 (A/0)Page 1/1 EC Declaration of ConformityManufacturer :whose single Authorized Representative:XXXXXXXXXXXX CO.,LTDXXXXXXXXXXXXXXXXXXXXXWe, the manufacturer, herewith declare that the products DISPOSABLE STERILE RETRACTABLE SAFETY SYRINGE UMDNS -Code: 12132; GMDN-Code/Preferred Terms: XXXXXmeet the provisions of Directive 93/42/EEC which apply to them.The medical device has been assigned to class IIa according to Annex IX of the Directive 93/42/EEC. It bears the mark0197The product concerned has been and manufactured under a quality management system according to Annex V of Directive 93/42/EEC.Compliance of the designated product with the Directive 93/42/EEC has been assessed and certified by the Notified BodyTÜV Rheinland LGA Products GmbHTillystraße 2, 90431, Nürnberg, GermanyCertificate No.: xxxxxxxxxIssue date: xxxxxxxxxExpiry date: xxxxxxxxxfollowing the procedure relating to the EC Declaration of Conformity set out in Annex V of Directive 93/42/EEC.This Declaration of Conformity covers all medical devices as specified in the product list belonging to this declaration and is only valid in connection with a batch specific Certificate of Compliance for all products concerned bearing the CE markThe above mentioned declaration of conformity is exclusively under the responsibility ofCompany: XXXXXXXXXXXXXXXXAddress: XXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXXPlace, date Legally binding signature, Function。

DECLARATION OF CONFORMITY我，(制造商名称) xxxx电气有限公司公司声明，(生产厂名称) xxxx电气有限公司生产的(详细填写产品名称、规格/型号) 动力柜SDXL主母线:In=630A～100A,Icw=10kA;Ue=380V,Ui=660V;50Hz;IP30符合如下要求：a) 中华人民共和国国家标准：____GB7251.1-2005_b) 其它相关标准或规定：_____________________________________________我公司对上述声明完全负责。

We,(manufacturer’s name)_ _ declare under our sole responsibility that the product (detailed description of product including name type or model)_________ ______ product in (factory’s name and address): _ _________ to which this declaration relates is in conformity with:a) GB standards; _b) And ot her standards and/or regulation________________________ _____________________(签署时间及地点) (负责人签名)(Place & Date of issue) (Name & Signature)DECLARATION OF CONFORMITY我，(制造商名称) xxx电气有限公司公司声明，(生产厂名称) xxxx电气有限公司生产的(详细填写产品名称、规格/型号) GGD主母线:In=1600A～630A,Icw=30kA;配电母线:In=630A,Icw=30kA;Ue=380V,Ui=660V;50Hz;IP30符合如下要求：a) 中华人民共和国国家标准：____GB7251.1-2005 _b) 其它相关标准或规定：_____________________________________________我公司对上述声明完全负责。

欧盟doc声明模板欧盟（European Union，简称EU）是由28个欧洲国家组成的政治和经济联盟。

在欧盟内部，有许多协议、规定和文件需要得到成员国的共同批准和遵守，以确保欧盟的一体化和良好的合作。

其中，欧盟的声明（doc声明）模板是一种常见的文件形式，用于表达欧盟在特定议题上的立场和行动计划。

本文将介绍欧盟doc声明模板的基本结构和常见内容，并探讨其重要性和应用领域。

一、欧盟doc声明模板的基本结构欧盟doc声明模板通常由以下几个部分组成：1. 标题：声明的标题通常简洁明了，能够清楚表达出文档的主题和目的。

2. 引言：引言部分主要介绍声明的背景和目的，概括性地描述相关问题的重要性和紧迫性。

3. 主体内容：主体内容是整个声明的核心部分，通常包括以下几个方面：- 问题陈述：明确列出当前存在的问题，以及问题可能导致的风险和挑战。

- 相关数据和调查：通过数据、统计和调查结果等方式，提供有关问题的客观证据和背景信息。

- 目标和原则：阐明欧盟在解决问题过程中的目标和原则，以及为了实现这些目标将采取的具体行动。

- 行动计划：详细描述欧盟将如何动员各成员国和利益相关方共同努力，以确保行动的一致性和效果。

- 时间表和里程碑：指定具体的时间表和里程碑，以便监测和评估行动计划的进展和成果。

4. 结论：结论部分总结整个声明的核心内容和要点，以及对未来的展望和期望。

5. 署名和日期：声明最后需要包括发表声明的组织或机构的署名和日期。

二、欧盟doc声明模板的常见内容欧盟doc声明模板的具体内容会因不同议题而有所不同，但通常涵盖以下几个方面：1. 问题陈述：明确列出当前存在的问题，以及问题可能导致的风险和挑战。

2. 目标和原则：阐明欧盟在解决问题过程中的目标和原则，以及为了实现这些目标将采取的具体行动。

3. 行动计划：详细描述欧盟将如何动员各成员国和利益相关方共同努力，以确保行动的一致性和效果。

4. 时间表和里程碑：指定具体的时间表和里程碑，以便监测和评估行动计划的进展和成果。

declaration of conformity模板Declaration of Conformity[Your Company Name/Logo][Company Address][City, State, Zip Code][Phone Number][Email Address][Website]Declaration of Conformity[Product Name/Model Number/Part Number][Product Description]Date: [Date of Declaration]To whom it may concern,We, [Your Company Name], hereby declare that the above-mentioned product complies with all applicable standards, regulations, and requirements set forth by the relevant authorities. This declaration of conformity is issued in accordance with the [Country or Region] regulations [Regulation Name or Number].1. Identification of the product:- Product Name/Model Number/Part Number: [Product Name/Model Number/Part Number]- Product Description: [Brief description of the product]2. Compliance Statement:- [Specify the standards, regulations, or directives that the product adheres to]- [List any relevant testing or certification bodies]3. Technical Documentation:- [Specify the technical documentation that supports the product's conformity]- [Provide reference to documents, such as test reports, safety guidelines, etc.]4. Manufacturer's Information:- Manufacturer's Name: [Your Company Name]- Manufacturer's Address: [Your Company Address]- Contact Person: [Contact Person's Name]- Contact Information: [Phone Number/Email Address]5. Authorized Representative (if applicable):- [Name of Authorized Representative]- [Address of Authorized Representative]- [Contact Information of Authorized Representative]6. Additional Information (if applicable):- [Include any additional information or statements regarding the product's conformity]We hereby declare that all the information provided in this Declaration of Conformity is accurate and true to the best of our knowledge. We take full responsibility for the conformity of the above-mentioned product.Sincerely,[Your Name][Position/Title][Your Company Name]。

符合性（自我）声明 - 针对EMC按符合性评定模式A进行评估的电子产品
需要更新为最新版的指令，
例如EMC 为2014/30/
EU，LVD为2014/35/EU.
符合性声明 - 针对已获得由公共机构出具EMC报告/证书的电子产品
需要更新为最新版的指令，
例如EMC 为2014/30/
EU，LVD为2014/35/EU.
符合性（自我）声明 - 针对在MD指令附录IV之外且按符合性评定模式A进行评估的机械产品
需要更新为最新版的指令，
例如EMC 为2014/30/
EU，LVD为2014/35/
EU，MD为2006/42/EC.
符合性声明 - 针对已获得由公告机构EMC报告/证书，且在MD指令附录IV之外且按符合性评定模式A进行评估的机械产品
需要更新为最新版的指令，
例如EMC 为2014/30/
EU，LVD为2014/35/
EU，MD为2006/42/EC.。

欧盟ce认证doc声明模板英文版篇 1The DOC declaration template for EU CE certification is of paramount importance! It ensures that products meet the strict standards set by the European Union. Let's take electronic devices as an example. For these products, the certification requires detailed tests on electrical safety and electromagnetic compatibility. The declaration must contain crucial information such as the manufacturer's name and address, a precise description of the product, and a clear statement indicating compliance with relevant standards. Isn't it essential to have this information accurately presented? Similarly, for medical devices, there are specific requirements regarding performance and biocompatibility. The manufacturer must provide detailed test reports and risk assessments. How important is it to follow these rules precisely to guarantee the safety and quality of the products? In conclusion, a well-prepared DOC declaration template is not only a legal requirement but also a guarantee of product quality and consumer safety!篇 2CE Certification DOC Declaration Template for the European UnionOh dear readers, let me guide you through this essential EU CE Certification DOC Declaration Template! Here's a simple yet clear template example for you: Declaration of ConformityWe, [company name], hereby declare that the product [product name], model [model number], complies with all the relevant essential requirements and other provisions of the applicable EU directives and regulations.The key points for filling each part are as follows. For the company name, itmust be the legal and registered name of your company. The product name and model number should be accurate and specific. But how to ensure the legality and validity of this declaration? Firstly, make sure you have conducted thorough testing and verification of your product to meet the EU standards. Secondly, keep all the relevant documentation and records for potential audits. Isn't it important to follow these steps carefully? So, with this template and explanations, you can now handle the CE Certification DOC Declaration with confidence!篇 3Oh dear friends! Let's talk about the EU CE Certification DOC Declaration Template. This template is of paramount importance! You know why? Imagine a company that filled it wrongly or incompletely. Their products were rejected from entering the EU market. What a disaster! This shows how crucial it is to fill it accurately. A correct and complete declaration template can open the door to the vast EU market for enterprises. It gives consumers confidence in the quality and safety of the products. Isn't that amazing? It helps build trust and boosts sales. So, dear friends, always take this template seriously and fill it with utmost care and precision. It's the key to success in the EU market!篇 4The EU CE Certification DOC Declaration Template is of vital importance in the European market! It serves as a guarantee of product compliance and quality. Different types of products indeed have distinct declaration template variations. For instance, electronic devices may have more detailed technical specifications compared to simple consumer goods. The reasons for template updates and changes are numerous. It could be due to evolving technological standards, new safety regulations, or changes in market demands. These updates have a significant impact! They ensure that products remain safe and meet the latest quality benchmarks. Butthey also pose challenges for manufacturers, as they need to stay updated and adapt their production processes accordingly. Isn't it essential for businesses to understand and comply with these changes to succeed in the EU market? Clearly, a thorough knowledge of the EU CE Certification DOC Declaration Template is crucial for all involved in the trade.篇 5The EU CE Certification DOC Declaration Template is a highly complex and significant document that plays a crucial role in ensuring the compliance and quality of products in the European market. It encompasses various elements, each with its own profound significance and legal basis. For instance, the requirements related to product safety and performance are based on strict and authoritative regulations such as the relevant directives and standards. These not only safeguard the interests of consumers but also maintain fair competition in the market.However, as the market and technological advancements continue to evolve, questions arise about the future of this template. Will there be more stringent requirements for emerging technologies? How will it adapt to changes in global trade patterns? It's highly likely that the template will undergo continuous refinement and improvement to keep pace with the times. Maybe there will be a greater emphasis on environmental sustainability and digital aspects. Isn't it fascinating to think about these possibilities? The EU CE Certification DOC Declaration Template is not just a formality; it's a dynamic tool that shapes the future of product compliance in the European Union!。

D e c l a r a t i o n-o f-C o n f o r m i t y-符合性声明--2010-M D D原件M ANUFACTURER: NAME AND ADDRESSM EDICAL D EVICE: NAME, TYPE AND / OR MODELOR S EE A TTACHED L IST - INCLUDE UMDNS AND/OR GMDN[NAME AND CODE]C LASSIFICATION -A NNEX IX: E.G.CLASS II A, RULE 11C ONFORMITY ASSESSMENT R OUTE: E.G.A NNEX VII+V.3W E, THE MANUFACTURER, HEREWITH DECLARE THAT THE STATED MEDICAL DEVICESMEET THE TRANSPOSITION INTO NATIONAL LAW, THE PROVISIONS OF C OUNCIL D IRECTIVE 93/42/EEC OF 14 JUNE 1993 CONCERNING MEDICAL DEVICES;INCLUDING, AT 21 MARCH 2010, THE AMENDMENTS BY C OUNCIL D IRECTIVE 2007/47/EEC.A LL SUPPORTING DOCUMENTATION IS RETAINED AT THE PREMISES OF THE MANUFACTURER.S TANDARDS APPLIED:EN ISO13485:2003/AC2007,EN ISO14971:2007,EN ISO11135-1:2007,EN ISO 11607-1,EN ISO11607-2,EN ISO10993-1:2003,EN556-1,EN1041:2008,EN980:2008以及适用的产品协调标准，至于有哪些标准，具体察看协调标准网站N OTIFIED B ODY:TÜV SÜD P RODUCT SERVICE G MB HR IDLERSTR 65,D-80339MÜNCHEN,G ERMANY IDENTIFICATION NUMBER 0123(EC)C ERTIFICATE(S): EC CERTIFICATE(S) NUMBER(S)SHOW ONLY THE EC CERTS WITH A SCOPE THAT COVERS THE PRODUCTS LISTEDE UROPEAN R EPRESENTATIVE: Shanghai International Trading Corp. GmbH (Europe)Eiffestrasse, 80, D-20537, Hamburg, Germany Tel: 0086-021-65951371，0049-40-2513175，Fax: 0049-40-255726S TART OF CE-MARKING: D ATE OF FIRST CE MARKING (OR LOT OR SERIAL NUMBER)USUALLY = ISSUE DATE OF EC CERT.(AND ADD END DATE - WHEN EC CERT. VALIDITY ENDS,OR WHEN DEVICE CEASES TO BE MARKETED, OR WHEN NB IS CHANGED)P LACE,D ATE OF D ECLARATION: CITY, DATES IGNATURE: ____________________NAME:POSITION:(RESPONSIBLE S ENIOR E XECUTIVE OF MANUFACTURER)。

certificate of conformity模板以下是一个简单的"Certificate of Conformity"（符合性证书）的模板示例：[公司名称] [公司地址] [城市，州/省，邮编] [国家] Certificate of Conformity This is to certify that the following product(s) have been tested and found to be in conformity with the specified standards and requirements: Product Information: - Product Name: [产品名称] - Model/Part Number: [型号/零件编号] - Batch/Serial Number: [批次/序列号] - Date of Manufacture: [制造日期] Conformity Details: - Standard(s) and Requirement(s): [适用标准和要求] - Test Method(s) Used: [使用的测试方法] - Test Date(s): [测试日期] The above-mentioned product(s) have successfully passed all applicable tests and meet the necessary quality and safety standards. This certificate is valid for a period of [有效期限] and applies only to the specified product(s) as mentioned above. Authorized Signatory: [签名] [日期] [公司名称] [公司联系信息]请注意，这只是一个简单的模板示例，你可以根据自己的需求和具体的情况进行修改和定制。

符合性声明英文版范文Declaration of Conformity.We, [Company Name], hereby declare that the product, [Product Name], conforms to the following essential requirements of the applicable European Directives:Directive 2014/30/EU (Electromagnetic Compatibility Directive)。

Protection against electromagnetic interference (Article 3.1(a))。

Minimum level of immunity to electromagnetic interference (Article 3.1(b))。

Directive 2014/35/EU (Low Voltage Directive)。

Protection against electric shock (Article 3)。

Protection against thermal hazards (Article 4)。

Directive 2011/65/EU (Restriction of Hazardous Substances Directive)。

Restriction of the use of certain hazardous substances in electrical and electronic equipment (Annex II)。

Directive 2012/19/EU (Waste Electrical and Electronic Equipment Directive)。

Proper disposal of waste electrical and electronic equipment (Article 4)。

eu declaration of conformity模板EU Declaration of Conformity模板是欧盟规定的一种产品合格性声明模板。

该模板详细描述了产品的规格、性能、生产厂商信息，以及符合的欧盟法规标准，是向消费市场销售的产品必须遵守的规定之一。

下面将分步骤阐述EU Declaration of Conformity模板。

1.产品信息在EU Declaration of Conformity模板中，需要明确标识产品的名称、型号、批次号等信息，以确保生产厂商的产品可以被准确地识别。

这些信息不仅有助于在市场上建立生产厂商和产品的良好声誉，而且还可以在必要时追溯产品的来源和质量，从而保障消费者权益。

2.制造商信息EU Declaration of Conformity模板还需要列出生产厂商的详细信息，包括公司名称、地址、联系方式等。

这些信息可以帮助消费者和监管机构在必要时找到并联系生产厂商，确认产品的真实性、合法性和符合性等方面的问题。

3.合规标准信息在EU Declaration of Conformity模板中，需要明确产品符合的欧洲法规标准，以确保生产厂商的产品能够符合欧盟的安全、健康、环保等法规标准。

对于不同的产品，需要符合不同的欧洲法规标准，例如机械设备指令、低压指令、电磁兼容性指令等。

生产厂商需要了解并遵守相应的法规标准，才能确保产品符合性。

4.测试报告信息在EU Declaration of Conformity模板中，还需要提供测试报告相关信息，以证明产品经过测试符合欧洲法规标准的要求。

测试报告应该提供相应的测试样本和具体的测试方法，以及测试结果和评价等信息，从而实现对产品符合性的充分证明。

5.声明信息在EU Declaration of Conformity模板的声明中，需要生产厂商确认产品符合欧洲法规标准，并愿意承担相关的责任和义务。

声明通常包括制造商名称、签名、日期等信息。

DECLARATION OF C ONFORMITYTO C OUNCIL D IRECTIVE 93/42/EEC OF 14 J UNE 1993CONCERNING M EDICAL D EVICESRef: EN ISO/IEC 17050-1 revision date: June 2009 M ANUFACTURER :NAME AND ADDRESSM EDICAL D EVICE :NAME , TYPE AND / OR MODEL OR S EE A TTACHED L IST - INCLUDE UMDNS AND /OR GMDN [NAME AND CODE ]C LASSIFICATION - A NNEX IX : E .G . CLASS II A , RULE 11C ONFORMITY ASSESSMENT R OUTE : E .G . A NNEX VII + V.3W E , THE MANUFACTURER , HEREWITH DECLARE THAT THE STATED MEDICAL DEVICES MEET THE TRANSPOSITION INTO NATIONAL LAW , THE PROVISIONS OF C OUNCIL D IRECTIVE93/42/EEC OF 14 JUNE 1993 CONCERNING MEDICAL DEVICES ;INCLUDING , AT 21 MARCH 2010, THE AMENDMENTS BY C OUNCIL D IRECTIVE 2007/47/EEC. A LL SUPPORTING DOCUMENTATION IS RETAINED AT THE PREMISES OF THE MANUFACTURER .S TANDARDS APPLIED : EN ISO 13485:2003/AC 2007, EN ISO 14971:2007, EN ISO 11135-1:2007, EN ISO 11607-1, EN ISO 11607-2, EN ISO 10993-1:2003, EN 556-1, EN1041:2008, EN 980:2008以及适用的产品协调标准，至于有哪些标准，具体察看协调标准网站N OTIFIED B ODY :TÜV SÜD P RODUCT SERVICE G MB HR IDLERSTR 65, D-80339 M ÜNCHEN , G ERMANYIDENTIFICATION NUMBER0123(EC) C ERTIFICATE (S ): EC CERTIFICATE (S ) NUMBER (S )SHOW ONLY THE EC CERTS WITH A SCOPE THAT COVERS THE PRODUCTS LISTEDE UROPEAN R EPRESENTATIVE : Shanghai International Trading Corp. GmbH (Europe)Eiffestrasse, 80, D-20537, Hamburg, Germany Tel: 0086-021-65951371，0049-40-2513175，Fax: 0049-40-255726S TART OF CE-MARKING : D ATE OF FIRST CE MARKING (OR LOT OR SERIAL NUMBER ) USUALLY = ISSUE DATE OF EC CERT .(AND ADD END DATE - WHEN EC CERT . VALIDITY ENDS ,OR WHEN DEVICE CEASES TO BE MARKETED , OR WHEN NB IS CHANGED )P LACE , D ATE OF D ECLARATION :CITY , DATES IGNATURE :____________________NAME :POSITION : (RESPONSIBLE S ENIOR E XECUTIVE OF MANUFACTURER )。

欧盟符合性声明模板EU DECLARATION OF CONFORMITY (No XXXX)欧盟符合性声明（No XXXX ）1. Pressure equipment or assembly (product, type, batch or serial number):1、压力设备或组合件（产品，类型，批号或序列号）：2. Name and address of the manufacturer and, where applicable, his authorised representative:2、制造商的名称和地址，以及他的授权代表（如适用）：3. This declaration of conformity is issued under the sole responsibility of the manufacturer.3、制造商自行负责制定本符合性声明。

4. Object of the declaration (identification of pressure equipment or assembly allowingtraceability; it may, where necessary for the identification of the pressure equipment or assembly, include an image):4、声明的对象（具有可追溯性的压力设备或组合件标识；当有必要识别压力设备或组合件时，它可以包含图片）：—description of the pressure equipment or assembly, ——压力设备或组合件的描述，—conformity assessment procedure followed,——合格评定程序，—in the case of assemblies, description of the pressure equipment constituting the assembly,and the conformity assessment procedures followed, ——在组合件的情况下，描述构成组合件的压力设备以及合格评定程序，5. The object of the declaration described above is in conformity with the relevant Unionharmonisation legislation:5、以上声明目的是满足相关欧盟协调法规：6. References to the relevant harmonised standards used or references to the other technical specifications in relation to which conformity is declared:6、引用使用的相关协调标准，或引用符合性声明相关的其他技术文件：7. Where appropriate, the name, address and number of the notified body which carried out the conformity assessment and the number of the certificate issued, and a reference to the EU-type examination certificate –production type, EU-type examination certificate –design type, EU design examination certificate or certificate of conformity.7、当合适时，进行合格评定公告机构的名称、地址和编号和颁发证书的编号，以及引用欧盟型式检验证书—生产型，型式检验证书—设计型，或符合性证书。