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Rules - MDD Advantages for PurchasersCE-marked medical devices comply with all relevant requirements of the Directive. Except for devices in class I, the CE marking will also be provided with a number which identifies the notified body that approved the product and/or the manufacturer's quality system.The CE mark is proof to the purchaser that the products are sufficiently safe and that they will function according to the specifications of the manufacturer. This means that further inquiry by the purchaser is not necessary and thus a reduction in the administrative workload may be anticipated. In case the purchaser is still not convinced that the product is safe, he may request the information available in the manufacturer's statutory technical documentation. Back to index |
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