MDSS 欧盟授权代表 MDSS 企业咨询   英语    德语    简体中文
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




符合性评估 (Conformity Assessment)


符合性评估 (Conformity Assessment)


根据欧盟指令规定,医疗器械产品必须符合欧盟指令中所提到的要求才能取得CE标志,从而在欧盟境内上市。CE标志代表着品质,它不仅可以帮助您打开欧盟市场的大门,更可以扩大产品在非欧盟市场的销售。


MDSS将协助您选择一套合适您的产品的评估程序,让您的产品顺利的取得CE标志。


如果您有任何需求,请随时联系我们。我们将非常乐意为您提供服务。




Contact us 请点击此处联系我们


返回主