Portable mesh nebulizer complies with European directives:
a) Directive 2006/95/EC of the European Parliament and of the Council relating to electrical equipment
designed for use within certain voltage limits
b) Directive 2014/30/EU of the European Parliament and of the Council on the harmonization of the
laws of the Member States relating to electromagnetic compatibility (recast)
c) Directive 2011/65/EU of the European Parliament and of the Council on the restriction of the use of
certain hazardous substances in electrical and electronic equipment
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8. Declaration of Conformity
9. Warranty
This device can only be assigned to the functions it has been designed for, i.e. nebulization. The
manufacturer cannot be held responsible for any damage deriving from improper, incorrect or
unreasonable use.
All our appliances have undergone strict inspection test and are guaranteed against manufacturing
defects. The guarantee starts from the date of purchase. The date of purchase is the date shown on the
invoice issued by the dealer upon the delivery of the appliance.
Evidence of original purchase is
required for warranty services, so it is important to keep your sales receipt.
The warranty period is applicable according to local country law and regulation in force.
The manufacturer undertakes to repair or replace cost-free within the warranty period those parts that
prove to have manufacturing defects. Those defects that are not clearly attributable to either material
or the manufacturing will be examined at one of ZEPTER Service Centres or at our headquarters and
charged according to the outcome.
