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Drug-eluting medical devices stents

A1 Lamee K and Cook D. Polymer coating techniques for drug eluting stent. Medical device technology 2003 http /www.medicalde vicesonline.com/ mdt/articledetail.j se =52234. [Pg.471]

The FDA defines the PMOA for a drug eluting stent (DBS) is as a device [38, 39]. During the regulatory process CDER would be involved with the review of the pharmacologic agent and CDRH would review the stent platform, the delivery system and the carrier (polymer), if present. In Europe a DES would also be viewed as a medical device [15,40]. [Pg.342]

Medical Device Technology 14, No. 1, Jan.-Feb.2003, p. 12-4 POLYMER COATING TECHNIQUES FOR DRUG-ELUTING STENTS... [Pg.68]

See other pages where Drug-eluting medical devices stents is mentioned: [Pg.93]    [Pg.67]    [Pg.188]    [Pg.81]    [Pg.354]    [Pg.195]    [Pg.289]    [Pg.618]    [Pg.240]    [Pg.354]    [Pg.247]    [Pg.647]    [Pg.208]    [Pg.239]    [Pg.380]    [Pg.5]    [Pg.433]    [Pg.436]    [Pg.133]    [Pg.185]   
See also in sourсe #XX -- [ Pg.185 , Pg.199 ]



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