Medical Devices Ordinance
(MedDO)


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Art. 22 Exemptions

1 On a duly jus­ti­fied re­quest, Swiss­med­ic may au­thor­ise the pla­cing on the mar­ket and put­ting in­to ser­vice of a spe­cif­ic device the use of which is in the in­terests of pub­lic health or pa­tient safety or health even though:

a.
the rel­ev­ant con­form­ity as­sess­ment pro­ced­ure in ac­cord­ance with Art­icle 23 has not been car­ried out; or
b.
the lan­guage re­quire­ments in Art­icle 16 para­graph 2 have not been met.

2 In­di­vidu­al devices that have not un­der­gone the rel­ev­ant con­form­ity as­sess­ment pro­ced­ure may be placed on the mar­ket and used without au­thor­isa­tion from Swiss­med­ic provided:

a.
they serve to avert life-threat­en­ing con­di­tions or to re­solve the per­man­ent impair­ment of a body func­tion;
b.57
no con­form­ing device is avail­able for this spe­cif­ic in­ten­ded pur­pose;
c.
they are used ex­clus­ively by health­care pro­fes­sion­als on in­di­vidu­al per­sons;
d.
the health­care pro­fes­sion­al us­ing the device has in­formed the in­di­vidu­al con­cerned about the non-con­form­ity of the med­ic­al device and the re­lated risks; and
e.
the in­di­vidu­al con­cerned has con­sen­ted to the use of the device.

3 For devices placed on the mar­ket ex­clus­ively with­in the armed forces or with­in the frame­work of their spe­cif­ic tasks, the Fed­er­al De­part­ment of Home Af­fairs (FDHA) may, in agree­ment with the Fed­er­al De­part­ment of De­fence, Civil Pro­tec­tion and Sport, grant ex­emp­tions.

57 Amended by An­nex 5 No 1 of the O of 4 May 2022 on In Vitro Dia­gnost­ic Med­ic­al Devices, in force since 26 May 2022 (AS 2022 291).

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