User's Manual

62 – US-ENGLISH
Non-serious events due to the use of SafeR included: delay in
switching on 2nd degree AV block, inappropriate classification of a
PAC, disagreement between markers and recorded EGM, atrial
pacing above the maximum rate, recycling on an r-wave in a
refractory period, and disagreement in the statistics for switches to
DDD. No patient symptoms were associated with these events.