eu marine equipment directive (med)-凯发k8国际首页登录

eu marine equipment directive (med)

directive 96/98/ec amending directive 94/25/ec on recreational craft was officially enforced on january 1, 1999. this directive covers all ships registered in eu member states. its primary objective is to ensure that marine equipment complies with the requirements agreed upon by the international maritime organization (e.g., solas) and meets the safety performance standards of the eu. approved requirements are used to coordinate and ensure that certificates signed by one member state are accepted by other eu member states.

 

the directive applies to groups of registered vessels and was formally enforced on january 1, 2001. on july 23, 2014, the eu issued directive 2014/90/eu, which revoked directive 96/98/ec from september 18, 2016. the marine equipment directive 2014/90/eu came into force on march 16, 2017. it specifically regulates the requirements for equipment intended for use on board vessels circulating within the european economic area, aiming to enhance maritime safety, prevent marine pollution, and ensure the circulation of such equipment within the european community.

 

as per the regulations of eu certification directives, eu-related directive certifications can only be carried out by designated bodies registered within the eu. upon obtaining eu authorization, these bodies can issue med certification for (mandatory) products used on eu-flagged vessels and grant the "wheelmark" symbol.

 

value gain

the ce certification provides a unified technical standard for products from various countries to trade in the european market, streamlining trade procedures. any product from any country intending to enter the european union or the european free trade association must undergo ce certification and bear the ce mark. therefore, ce certification serves as a passport for products entering the markets of european union and european free trade association countries. it signifies that the product meets the safety requirements set by the european union directives. it's a commitment from businesses to consumers, enhancing consumer trust in the product. products bearing the ce mark will reduce risks associated with sales in the european market.

service process

1.application submission
2.application confirmation
3.submission of technical documents
4.technical document review and product testing
5.certificate issuance

q&a
 
what are the various assessment modes for ce certification under the marine equipment directive (med) for marine equipment?

the ce certification under the marine equipment directive (med) offers different certification modes for various maritime equipment. the main modes are as follows:

(1) module b: type-examination

(2) module d: production quality assurance

(3) module e: quality assurance

(4) module f: product verification

(5) module g: unit verification

how to understand module b certification?
module b certification, known as ec type-examination (formal type approval), involves eu notified bodies reviewing equipment technical data alongside conducting tests on selected samples based on relevant standards. certification engineers witness the entire testing process. upon successful completion of both technical data review and sample testing, the notified body certifies that the equipment sample complies with the med directive and issues a module b certificate.
how is the module b type examination specifically carried out?

(1) initial review of the product's technical documentation to preliminarily verify compliance with directive requirements.

(2) testing of selected samples, witnessing the entire testing process, recording test data, and evaluating the test results.

(3) checking whether the standards used for technical data review and sample testing have been correctly applied by the manufacturer.

(4) manufacturers make necessary adjustments or improvements to technical documentation or samples, conducting retesting if needed until both technical data review and sample testing are successfully completed.

how long is the validity period of module b certificate?
the validity period of a module b certificate is 5 years.
our advantage
authoritative qualification
noa has been approved by certification and accreditation administration of the people’s republic of china(cnca)(cnca-r-2002-051), and has obtained qualification of china inspection body and laboratory mandatory approval (cma),and has passed the multiple approvals of china national accreditation service for conformity assessment (cnas), international accreditation service (ias), united kingdom accreditation service (ukas), joint accreditation system of australia and new zealand (jas-anz). noa has been approved by state administration for market regulation of china, and has been recognized as inspection and testing institution of china's special equipment, as well as the qualification of china's national equipment supervision and engineering supervision. noa-dci is the notified body of the ce directive of the european commission. noa has been recognized by the international electrotechnical commission (iecq) by obtaining electronic component quality assessment system. it is also a national inspection and assessment notified body of import and export commodity in china.noa is a high-tech enterprise in shanghai.
improve performance, realize asset value appreciation, and service throughout the entire value chain
from pre-design to post-operation, noa has the ability to guarantee the whole life cycle of the business. noa, as an independent third-party inspection company, has a large number of domestic and international standards and specifications proficient in design, welding, non-destructive testing, painting, packaging and other fields the experienced team of professional engineers and inspection experts, with more than ten years of experience in the domestic market, is familiar with all aspects of the domestic industrial equipment supply chain, and can provide you with technical support services for the full life cycle of technical services in a timely manner, combining various products. inspection, certification, testing, consulting, and auditing services can provide you with one-stop all-round comprehensive services.
quality, efficiency and service
noa has formed a mature and solid operation system in the development of more than 20 years. we let technical experts who are familiar with market regulations and testing standards and have professional industry experience to carry out inspection, evaluation and design review work. while meeting the requirements of domestic and international standards, we ensure that customers can obtain satisfactory service results in the first time with accurate time-sensitive management methods, and ensure that customers can seize the opportunity in the market competition.
service area
noa inspection services currently cover europe, australia, russia, some middle east regions and most regions in china. noa can ensure the consistency and continuity of customer service in different regions, and eliminate the impact of unfamiliar environments on customer quality. the guarantees and the impact of project implementation enable customers to participate in different markets across the country or around the world with flawless quality.
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