11
Standards
The device complies with the specifications of EU
Directive 93/42/EEC for medical products and with the
national laws on medical products.
The device complies with the requirements of Directive
1999/5/EC (R&TTE). The monitor visibly bears the CE
mark.
The monitor fulfills Directive 2002/95/EC of the
European Parliament and the European Council of 27
January 2003 on restricting the use of specific
hazardous materials in electrical and electronic
equipment.
12
Warranty and repairs
Warranty information
I.E.M. GmbH provides a two year warranty on the
blood pressure monitor from the date of sale. Proof
of the date of sale shall be provided in the form of a
properly completed warranty card or an invoice.
Faults due to material or production defects shall be
remedied free of charge within the warranty period.
A warranty claim does not result in an extension of
the warranty period, neither for the device nor for
the replaced components.
The following are excluded from the warranty:
All damage caused by improper handling, e.g. by
non-compliance with the operating instructions.
Damage resulting from maintenance or
intervention by the purchaser or unauthorized
third parties.
Transport damage on route from the manufacturer
to the consumer or during shipment to the
customer service.
Accessory parts subject to normal wear and tear
(cuff, batteries, etc.).
Standards
EN
75