CE Marking For Sterilization And laboratory Equipments

Eurotech Certification Body Provide CE marking Certification Service on Sterilization And laboratory Equipment's As Per CE Mark-IVD (IVD-In Vitro Diagnostic Medical Devices)European IVD Regulatory Approval Process, In Europe, the In-Vitro Diagnostic Devices Directive (98/79/EC)

Eurotech and Meddevices can audit and certify your organization against 98/79/EC to enable use of the IVD CE Mark on your products.

Eurotech Certification Body IVD experts can assist you in complying with the In-vitro Diagnostic Device Directive 98/79/EC. Our affordable and practical approach to CE Marking for Medical Devices

Understanding the In Vitro Diagnostic Medical Devices Directive (98/79/EC). EU In vitro diagnostic medical devices (IVDs) are subject to the European Directive

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

Best Regards,
Puneet Sharma 
08196980555