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EU MDR
Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC/ has now come into place.
Jumapanilo SL is able to assist manufacturers and clients located outside the EU in obtaining the necessary documentation and representation to enable their medical and sanitary products to be sold within the European Union.
JUMAPANILO SL
EUDAMED SRN : ES-AR-000004849
Contact us for more information on how we can assist your organisation.
CLIENT INFORMATION
EU MDR: About
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