CE marking and CE certification
- 1. CE Marking Consultants For Medical Device
- 2. / Who Can Apply For CE Marking?
- 3. CE marking for the electrical, electronic and medical device says that the manufacturer claims that a product meets all the essential requirements of all relevant European Medical Device Directives and makes it ready for its usage to the customers. MedDeviceCorp has tested and provided thousands of products to support CE Marking and CE certification for product safety, electromagnetic compatibility, and energy efficiency. Contact us today to tap the experience and skill of our CE expertise team and get quick Medical Device CE Marking.
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- 5. / What is the CE mark
- 6. / CE marking is the medical device manufacturer's claim that a product meets the essential requirements of all relevant European Medical Device Directives. The Directives outline the saftey and performance requirements for medical devices in the European Union (EU).
- 8. CE Marking Steps to CE marking by the CE marking consultants: 1. Identify the relevant directives and its standards 2. Verify the product’s specific requirements 3. Identify whether an independent conformity assessment (Notified Body Medical Device) is necessary or not 4. Test the product 5. Create the technical documentation 6. Finally, Add the CE mark to the specific product
- 9. ● CE Marking ● ISO 13485 ● FDA 510(k) ● Cleanrooms ● GMP certificate ● Drug Master File ● US FDA Registration, and etc. Medical Device
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- 16. Contact Us Visit: http://www.meddevicecorp.com/ Call +44 2037594094 75 Executive Drive, Suite 303, Aurora, Illinos – 60504
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