Medical Devices Ordinance
(MedDO)

English is not an official language of the Swiss Confederation. This translation is provided for information purposes only and has no legal force.

of 1 July 2020 (Status as of 26 May 2021)


Open article in different language:  IT
Art. 48 Document retention requirements

1 Man­u­fac­tur­ers must en­sure that the fol­low­ing are avail­able to the com­pet­ent au­thor­ity for at least ten years after the fi­nal product covered by the de­clar­a­tion of con­form­ity has been placed on the mar­ket:

a.
com­plete tech­nic­al doc­u­ment­a­tion;
b.
de­clar­a­tion of con­form­ity;
c.
a copy of the cer­ti­fic­ates is­sued, in­clud­ing any amend­ments and ad­denda.

2 The doc­u­ment re­ten­tion peri­od for im­plant­able products shall be at least 15 years from the date the last product was placed on the mar­ket.

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