Technical Information; Manufacturer; Declaration Of Conformity - I-Tech MIO-CARE TENS Manual De Usuario

Consult your doctor before using MIO-CARE, if you suffer from health problems.
Read carefully the user and the electrode positioning manuals before using
Read carefully contraindications and warnings.

Manufacturer

IACER Srl. is an Italian manufacturer of medical devices (certified CE no. MED24021
from the Notified Body no. 0476, Kiwa Cermet Italia Spa).

Declaration of conformity

Via S.Pertini 24/A – 30030 Martellago (Ve), Italia
herewith declares under its own responsibility, that the product
has been designed and manufactured according to the European Medical
Device Directive 93/4/EEC (transposed in Italy by the D.Lgs. 46/97), as
modified by the Directive 2007/47/EC (D.Lgs.37/2010) and further
modifications/integrations.
The product has been assigned to class IIa, according to Annex IX, rule 9 of
the Directive 93/42/EEC (and further modifications/integrations) and bears
the mark
IACER Srl
WARNING: MIO-CARE IS A MEDICAL DEVICE.
MIO-CARE.
I.A.C.E.R. S.r.l.
Via S. Pertini, 24/a • 30030 Martellago (VE)
Tel. 041.5401356 • Fax 041.5402684
I.A.C.E.R. S.r.l
MIO-CARE TENS
MIO-CARE FITNESS
MIO-CARE BEAUTY
UMDNS Code: 13762
Batch no.:
Series no.:
61

Technical information

MNPG95