Radiological Protection Ordinance
(RPO)

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

of 26 April 2017 (Status as of 1 January 2022)


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Art. 95 Further requirements for placing on the market

1 Be­fore be­ing placed on the mar­ket, every sealed ra­dio­act­ive source must be tested for leak tight­ness and ab­sence of con­tam­in­a­tion. Test­ing must be car­ried out by a body ac­cred­ited for this activ­ity or re­cog­nised by the su­per­vis­ory au­thor­ity.

2 The cap­sule of sealed ra­dio­act­ive sources whose activ­ity is great­er than 100 times the li­cens­ing lim­it must com­ply with the re­quire­ments of ISO 291935 for the in­ten­ded ap­plic­a­tion and be clas­si­fied ac­cord­ingly.

3 In jus­ti­fied cases, the su­per­vis­ory au­thor­ity may grant ex­emp­tions from para­graphs 1 and 2 or re­quire ad­di­tion­al qual­ity tests.

35 ISO 2919: 2012-02-15, Ra­di­olo­gic­al pro­tec­tion – Sealed ra­dio­act­ive sources – Gen­er­al re­quire­ments and clas­si­fic­a­tion. The ISO stand­ards re­ferred to in this Or­din­ance can be con­sul­ted free of charge at the Fed­er­al Of­fice of Pub­lic Health, CH 3003 Bern. They can be pur­chased from the Swiss As­so­ci­ation for Stand­ard­isa­tion, Sulzer­allee 70, 8404Win­ter­thur; www.snv.ch.

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