Procedure packs with non-medical devices

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Aside from under article 22, Is it possible for a non-medical device, let’s take biocides for example, to be included in a medical device pack that is CE marked under article 52, which means the non-medical product (biocide) is included in the ce mark. Would the biocide have to still meet biocides eu regulations? Or would the biocide be treated as a medical device component?
 
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