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CE marking must not be affixed to SEP equipment. Why is this the case when a manufacturer uses Conformity Assessment Procedure Module A for both his SEP and Category I products?

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CE marking must not be affixed to SEP equipment. Why is this the case when a manufacturer uses Conformity Assessment Procedure Module A for both his SEP and Category I products?

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The absence of a CE mark on SEP products will cause the user to question whether the equipment complies with the PED, even when it does!

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