54
The customer must inform the warrantor or the vendor of any faults within reasonable
time from when he or she detected them or should have detected them. When reporting
a fault, the customer must present a certificate of warranty, a receipt of purchase, or
another reliable account of where and when the product was purchased.
The warrantor or a service company authorised by the warrantor may choose to either
repair the fault or provide the customer with a faultless device within reasonable time
from receipt of the customer’s report on the fault. The customer may not invoke the
warranty if the device has been modified or if it has been repaired by a party other than a
service company authorised by the warrantor.
The warranty does not restrict the customer’s right to application of any consumer
protection legislation in force.
The device manufacturer can be contacted by post or by e-mail at the following
addresses:
VALKEE OY, Kauppiaantie 30, FI-90460 Oulunsalo, Finland
[email protected]
Limitation of risk
The warranty does not restrict the customer’s statutory rights or any other rights the
customer has in relation to the vendor.
The manufacturer’s liability is always restricted to the purchase price of the device. The
manufacturer is under no circumstances liable for compensation for any incidental,
indirect, or consequential damages unless legislative requirements impose an obligation
Summary of Contents for NPT 1100
Page 1: ...NPT 1100...
Page 5: ...5 Laite t ytt l kint laitedirektiivin 93 42 ETY vaatimukset...
Page 6: ...6 Laiteseloste Laitteen osat Kuva 1...
Page 8: ...8 Kuva takakannesta ja siell olevien symbolien selitykset Kuva 2...
Page 20: ...20...
Page 23: ...23 Apparaten uppfyller kraven i direktivet om medicintekniska produkter 93 42 EEG...
Page 24: ...24 Beskrivning av apparaten Apparatens delar Bild 1...
Page 38: ...38...
Page 41: ...41 The device meets the requirements of the medical device directive 93 42 EEC...
Page 42: ...42 Product description Device components Figure 1...
Page 44: ...44 A picture of the back cover with explanations of the symbols Figure 2...
Page 56: ...56...
Page 59: ...59 Das Ger t entspricht den Anforderungen der Richtlinie 93 42 EWG ber Medizinprodukte...
Page 60: ...60 Produktbeschreibung Ger tekomponenten Abb 1...
Page 78: ...78 Description du produit Composants du dispositif Figure 1...
Page 95: ...95 Het toestel voldoet aan de vereisten van de richtlijn 93 42 EEC inzake medische toestellen...
Page 96: ...96 Productbeschrijving Onderdelen van het toestel Afbeelding 1...
Page 113: ...113 Apparatet oppfyller kravene for medisinsk utstyr i direktiv 93 42 E F...
Page 114: ...114 Produktbeskrivelse Apparatets komponenter Figur 1...
Page 128: ...Kauppiaantie 30 FI 90460 Oulunsalo www valkee com...