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J. Ne xez pas le capteur avec du ruban adhésif ou similaire, car cela
pourrait provoquer la détection de la pulsation veineuse et donc des
mesures de
SpO2
erronées.
M. Veillez à ce que la surface optique soit libre de tout obstacle ou em-
pêchement.
N. La lumière ambiante excessive peut affecter le résultat de la mesure.
Cela comprend les lampes uorescentes, les radiateurs à infrarouge,
les rayons directs du soleil, etc.
O. Les mouvements énergétiques du patient ou l'interférence excessive
électro-chirurgicale peuvent affecter la précision de mesure.
3. SPÉCIFICATIONS TECHNIQUES
A. Modalità Display:
Afchage OLED
B. Exigences de puissance :
1 batterie rechargeable 3.6V LiR2450
Tension d'alimentation: 3.3V ~ 4.2V
Temps de travail continu: 4 heures
C. Courant d'alimentation : <= 40mA
D. Mesure SpO2 :
Intervalle de mesure : 35% - 100%
Précision ≤3% (pour valeurs entre 70% et 100%)
E. Mesure fréquence cardiaque :
Intervalle de mesure : 30 bpm - 240 bpm
Précision fréquence cardiaque : ±2bpm ou ± 2%
F. Mesure indice de perfusion :
Intervalle de mesure : 0% - 20%
G. Performance dans des conditions de faible perfusion
La précision des mesures de
SpO2
et de PR continue de répondre
aux spécications décrites ci-dessus lorsque l'amplitude de la mo-
dulation est de 0,6%.
H. Résistance aux interférences de la lumière ambiante :
La précision des mesures de
SpO2
et de PR continue de répondre
aux spécications décrites ci-dessus lorsque le dispositif est testé
par le simulateur de
SpO2
(série Fluke Biomedical Index 2) lors du
réglage des interférences d'émulation de la lumière solaire et de la
FRANÇAIS
22


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