Thursday, 3 December 2015

US FDA Registration for Medical devices



US FDA Registration and CE Marking  for Medical devices

Meddevices Providing CE Marking, ISO 13485, U.S FDA 510k, U.S FDA Registration, 21 CFR 820 Consulting Services.

Eurotech offer complete solutions for CE Marking your devices by offering the following services

1. Technical Consultancy
2. Documentation (Technical File Preparation)
3. Product Testing
4. GAPS Analysis/ Review of Technical File
5. Notified Body Audit and Certification.

Interested Manufacturers , Suppliers, Traders, Exporters can drop their requirements with product technical details at (Meddevices.net@Gmail.Com)

 Thanks & Regards, 
Puneet Sharma 
M: +91.8196980555 
Email id: SEO@eurotechworld.net, ce.marking.certification@gmail.com 
Eurotech ACS Pvt. Ltd. 
http://www.eurotechworld.net/, http://www.ce-marking-india.blogspot.in/, https://cemarkingexperts.wordpress.com/, http://www.meddevices.net/

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Location: India

4 comments:

  1. David9 December 2020 at 02:48

    Nice Blog

    FDA Certification

    ReplyDelete
  2. Healthy&Tasty26 March 2021 at 03:43

    CE Marketing is the Certification that ensures the products comply with health, safety and environmental protection, getting this CE certification in turkey marking declares that Products are manufactured with European safety and quality requirements.
    CE certification in turkey

    ReplyDelete
  3. Aishah Mahsuri15 February 2022 at 05:12

    Thanks for sharing!
    CE Mark certification

    ReplyDelete
  4. sk17 April 2022 at 08:22

    I just want to thank you for sharing your information and your site or blog this is simple but nice Information I’ve ever seen i like it i learn something today. FDA Certification

    ReplyDelete

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