Handling Instructions - BIOTRONIK Reocor S Gebrauchsanweisung

55
Users
Mode of action
Intended use
Changes not
permitted
Replacement parts
and accessories
Devices
on hand

General Description
Complications when inserting transvenous leads
include: Wound infection, arterial puncture, pericar-
dial friction, cardiac perforation and dysrhythmia after
lead insertion.

Handling Instructions

Depending on the pacing settings and the patient's
underlying illness, pacing can induce arrhythmias. To
ensure the patient's safety, certain procedures should
be observed and the precautionary measures listed
below taken. Please read about additional procedures
and precautionary measures in appropriate medical
publications.
• Reocor S may only be used by persons with
knowledge of cardiology who were trained in the
handling of the device. Potential users are techni-
cal and medical hospital staff and physicians.
• Reocor S interacts with the human heart. There is
also an interaction with the patient's skin and
blood vessels.
• Reocor S and the cables and accessories approved
along with the device may only be used in accord-
ance with this technical manual.
• Reocor S must not be connected to other electro-
medical devices.
• Reocor S must not be used in areas with a danger
of explosion.
• Only the manufacturer or a party expressly 
authorized by BIOTRONIK may perform corrective
maintenance, enhancements or modifications to
the device.
• To ensure safety compliance, use only original
replacement parts and accessories authorized by
BIOTRONIK. Using any other parts voids the 
manufacturer's liability for any consequences,
guarantee and warranty.
• In case of pacemaker dependency of the patient,
an emergency pacemaker should be kept on hand.