Technical Information; Manufacturer; Declaration Of Conformity - I-Tech MIO-CARE TENS Notice D'utilisation

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 S.r.l. is an Italian manufacturer of medical devices (certified CE n°
0068/QCO-DM/234-2020 from the Notified Body n° 0068 MTIC InterCert S.r.l.).

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
Compliance of the concerned product with the Directive 93/42/EEC has been
assessed and certified by the Notified Body:
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
0068 – MTIC InterCert S.r.l.
Via G. Leopardi 14, Milano (MI) 20123, Italia
Certified number: 0068/QCO-DM/234-2020

Technical information

64 MNPG95-05