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/
