IHT Cordynamic Hunter Bedienungsanweisung Seite 4

4.7. Open the haemostatic valve and move the new device forward whilst the guide is kept fixed in position in the coronary artery. Be careful
not to bend or rotate the device around the guide.
4.8. Move the new device forward and operate according to manufacturer instructions.
9. Warnings about re-use
Contents are supplied STERILIZED by ethylene oxide (EO). Do not use if the sterile barrier is damaged. If damage is detected, call an Iberhospitex
agent.
For single use in a single patient. Do not re-use, re-process or re-sterilise. Re-use, re-processing or re-sterilisation can affect the structural integrity
of the device and/or cause its failure, which in turn could cause injuries to the patient, disease or death. Re-use, re-processing or re-sterilisation can
also create a risk of device contamination and/or cause infection or cross infection to the patient, including but not limited to the transmission of
infectious diseases from one patient to another. Contamination of the device can cause injuries, disease or the death of the patient.
10.Warranty
Iberhospitex is not liable for damages caused to patients by misuse of the catheter; therefore, no claims will be accepted except for those stated in
this document. Under no circumstances will Iberhospitex be liable for any damage caused, except for those specifically established by the law.
The information provided in this package insert is a general description of the product and does not entail any express warranty for use. This information
is based on current knowledge of the product and medical science.
Explanation of the symbols used on the package labels:
Valid for a single use.
See Instructions of use before using this product.
Sterilised with ethylene oxide.
REF Reference number
LOT
Batch number
Use before
Ø
External diameter
Manufacturer