Technical Specifications; Manufacturer; Declaration Of Conformity - i-tec MAG1000 Mode D'emploi

Manufacturer

Via S. Pertini, 24/a • 30030 Martellago (VE) ITALY
IACER S.r.l. is an Italian medical devices manufacturer (CE medical certificate n°
MED24021).

Declaration of Conformity

IACER S.r.l., headquartered in Italy, via S. Pertini 24/A 30030 Martellago (VE),
declares on its own responsibility that MAG1000 is manufactured in conformity with Directive
93/42/EEC (MDD), Annex II as modified by Directive 2007/47/CE dated 5 September
2007 (D. Lgs. 37/2010 dated 25 January 2010).
Notified Body: Cermet, Via di Cadriano 23 – 40057 Cadriano di Granarolo (BO) Italy
MAG1000 is a Class IIa equipment, with reference to Directive 93/42/EEC (MDD),
annex IX rule 9 (and following modifications).
Martellago, 21/03/2010
IACER S.r.l.
I.A.C.E.R. S.r.l.
Tel. 041.5401356 • Fax 041.5402684
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Technical
Specifications
Legal representative
Mario Caprara
MNPG10 Rev. 06 Ed. 21/03/2010