Şunu aradınız:: pripomočkih (Çekçe - İngilizce)

oktobra 2001 o medicinskih pripomočkih (ro 2001 3487), kakor je bil nazadnje spremenjen 18.
| ordinance of 17 october 2001 on medical devices (ro 2001 3487), as last amended on 18 may 2005 (ro 2005 2695).

oktobra 1998 o in vitro diagnostičnih medicinskih pripomočkih (ul l 331, 7.12.1998, str.
1), as last amended by regulation (ec) no 1882/2003 of the european parliament and of the council of 29 september 2003 (oj l 284, 31.10.2003, p.

decembra 2000 o zdravilih in medicinskih pripomočkih (ro 2001 2790), kakor je bil nazadnje spremenjen dne 20.
| federal law of 15 december 2000 on medicinal products and medical devices (ro 2001 2790) as last amended on 20 december 2006 (ro 2006 5599).

junija 1990 o približevanju zakonodaje držav članic o aktivnih medicinskih pripomočkih za vsaditev, kakor je bila nazadnje spremenjena z uredbo (es) št.
| council directive 90/385/eec of 20 june 1990 on the approximation of the laws of the member states relating to active implantable medical devices, as last amended by regulation (ec) no 1882/2003 of the european parliament and of the council of 29 september 2003 (oj l 284, 31.10.2003, p.

za Švico je postopek za uradno sprostitev serij določen v členu 17 zveznega zakona o zdravilih in medicinskih pripomočkih ter v členih 18-21 odloka Švicarskega urada za terapevtske izdelke o zahtevah za dovoljenje za promet z zdravili.
for switzerland, the official batch release procedure is specified in article 17 of the federal law on medicinal products and medical devices and in articles 18-21 of the ordinance of the swiss agency for therapeutic products on the requirements for the marketing authorisation of medicinal products.

februarja 2003 o ponovni klasifikaciji prsnih vsadkov v okviru direktive 93/42/egs o medicinskih pripomočkih (ul l 28, 4.2.2003, str.
| commission directive 2003/12/ec of 3 february 2003 on the reclassification of breast implants in the framework of directive 93/42/eec concerning medical devices (oj l 28, 4.2.2003, p.

1774/2002 evropskega parlamenta in sveta v zvezi z uvozom in tranzitom nekaterih vmesnih proizvodov, pridobljenih iz snovi kategorije 3 in namenjenih za tehnično uporabo v medicinskih pripomočkih, in vitro diagnostičnih medicinskih pripomočkih in laboratorijskih reagentih, ter o spremembi te uredbe (ul l 379, 28.12.2006, str.
| commission regulation (ec) no 2007/2006 of 22 december 2006 implementing regulation (ec) no 1774/2002 of the european parliament and of the council as regards the importation and transit of certain intermediate products derived from category 3 material intended for technical uses in medical devices, in vitro diagnostics and laboratory reagents and amending that regulation (oj l 379, 28.12.2006, p.