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最新动态
  • Looking for a suitable GMDN-Code?
    MDSS can assist you to determine an appropriate code for your products!
    more


  • MDSS, may support you with the process of applying for a Certificate of Marketability...more


  • Update to IVD Directive...more

  • Update to MEDDEV Guidelines...more

  • Update to Portuguese Registration...more

  • Update to Vigilance Guideline...more

  • Update Harmonized Standards

    EN 980 is back...more



    
展会信息
Keep up to date!

News and Views March 2017

New Medical Device Regulation (MDR) in Europe
Read more...

In-House Workshops
The "NEW CE" mark
Book now!
 to make sure you’re ready to survive and thrive



重要事件
Meet us!

8. Medical Device Networking Meeting
Hanover, April 27, 2017




联系我们
MDSS GmbH
Schiffgraben 41
30175 Hannover
Germany

Phone
(+49)-511-6262 8630
FAX
(+49) -511-6262 8633

Click here to
contact us




技术文件 (Technical Documentation)


  • 文件 (Technical Documentation)

技术性文件是让产品符合欧盟指令的重要部分。随着产品的更新和变动,此类文件也必须相应并及时的被改动。


MDSS可以按照客户的需求提供相应的服务,比如文件的建立,文件的修改,更新等等。


如果您有任何问题,请随时联系我们。我们将非常乐意为您提供服务。





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