47
After the device has been removed from use, take it to a collection point for waste
electrical and electronic equipment. For further instructions, see the section
‘Removing the device from use’.
If a third party makes any modifications to the device itself or to its software, the
warranty becomes void.
If you do not charge the device battery via your computer’s USB port by means of the
supplied USB cable, use the optional USB charger sold by VALKEE Oy that is
intended for the charging of medical devices (this charger is not included in the
package). Use of any other chargers is prohibited.
Recommendations for use
The device is pre-set with a 12-minute treatment duration. Treatment safety has been
tested for one treatment every 24 hours. The recommendation is one 6–12-minute
treatment session per 24 hours. The longest treatment duration allowed is 12 minutes
each 24 hours. Do not exceed this maximum daily treatment duration.
Research shows that daily use alleviates symptoms of seasonal affective disorder in 1–4
weeks. However, the effects of the device vary greatly from one individual to another.
The most common side effects include a burning sensation in the auditory canals,
temporary headache at the beginning of treatment, insomnia, restlessness in the
evenings, decreased quality of sleep, and sleeplessness during the small hours. Any
sleeping disorder symptoms are primarily caused by the treatment time not being
suitable for the user in question. They usually disappear if the treatment time is changed
(for example, moved from morning to evening or vice versa).
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...
