Quality assurance forum
Registration with foreign Ministries
The CE marking of all Medical Devices manufactured by Spencer Italia S.r.l., has been carried out as specified in the MDD 93/42/CE (and following revisions ) and with the application of the technical requirements specified in the applicable normatives.
Thanks to this our products can circulate freely within the European Community.
Medical Devices sold in the countries outside the European Community have undergone the processes of evalutation and are compliant to the requirements of the laws of the local Authorities.
In the section Documents/International Registrations certificates of Spencer products issued bu Local Authorities can been consulted.
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