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giovedì, 29 ottobre 2009
FDA Registration

Spes medica s.r.l has registered medical devices to the FDA  (Food and Drugs Administration). The devices recorded represent the company core business: Disposable Concentric Needle electrodes MYOLINE, Disposable Needle for Botulin toxin injection MYOBOT and monopolar needle for EMG.

 

Link to the FDA web site

 


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©2008-09 Spes Medica S.r.l. P.IVA 03813040106 Via Europa Zona Industriale 84091 Battipaglia (Sa) tel. +39 0828 614191 fax + 39 0828 341788 info@spesmedica.com Credits www.dpsonline.it