CE MARKING CERTIFICATE
The CE marking as it has been legally called since
1993 (per directive 93/68/EEC) (Decision 93/465/EEC), or formerly EC mark is a mandatory conformity marking for
products placed on the market in the European Economic Area (EEA). With the CE marking on a
product, the manufacturer declares that the product conforms with the essential
requirements of the applicable EC directives.
DE system can help you gain easier access into the European market by ensuring your product meets all the CE mark requirements. If you manufacture or import products which fall into the scope of one or more of the New Approach Directives you will then need professional guidance on how to meet all the essential requirements of these directives. Before you can sell a medical device or IVD within Europe, you must obtain CE Marking certification and place a CE Mark (CE Marking) on your product. The CE Marking for medical devices is not a quality mark nor is it intended for consumers. It is a legally binding statement by the manufacturer that their product has met all of the requirements of the Medical Devices Directive (MDD 93/42/EEC), In Vitro Diagnostic Device Directive (IVDD 98/79/EC) or the Active Implantable Medical Device Directive (AIMDD 90/385/EEC), where applicable. If a Notified Body is required, the Notified Body's four-digit number would appear below the CE Marking symbol.
DE system can help you gain easier access into the European market by ensuring your product meets all the CE mark requirements. If you manufacture or import products which fall into the scope of one or more of the New Approach Directives you will then need professional guidance on how to meet all the essential requirements of these directives. Before you can sell a medical device or IVD within Europe, you must obtain CE Marking certification and place a CE Mark (CE Marking) on your product. The CE Marking for medical devices is not a quality mark nor is it intended for consumers. It is a legally binding statement by the manufacturer that their product has met all of the requirements of the Medical Devices Directive (MDD 93/42/EEC), In Vitro Diagnostic Device Directive (IVDD 98/79/EC) or the Active Implantable Medical Device Directive (AIMDD 90/385/EEC), where applicable. If a Notified Body is required, the Notified Body's four-digit number would appear below the CE Marking symbol.
For CE marking contact no. 91-9654656507, 9718380800
Email: desystemindia@gmail.com
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