Email *

Customer Name Surname *

Model/Serial Number *

1-Does the temperature on the external surface of the device reach levels that prevent contact? *
YesNo

2-Did the dry air sterilisation indicator used to test the sterility of the device show insufficient sterilisation? *
YesNo

3-During the sterilisation process, have you experienced any problems with the sterilisation stopping/interrupting due to the device? *
YesNo

4-During the verification process, did any problems occur regarding the accuracy of the set temperature value? *
YesNo

5-Has a problem occurred with uncontrolled increase/decrease of the temperature set on the display? *
YesNo

6-Is the buzzer on the device at a sufficient level? *
YesNo

7-Is the visual warning on the device sufficient? *
YesNo

8-Has there ever been a situation where the alarm was not activated despite the occurrence of the alarm conditions written in the user manuals such as "temperature exceeding the set alarm limits, start or end of sterilization time"? *
YesNo

9-Were there any problems with the legibility of temperature and time data on the screen of the device used? *
YesNo

Other Comments and Suggestions on Product Safety and Performance

Email *

Customer Name Surname *

Model/Serial Number *

1-Does the output power of the electrocautery device achieve the desired (cutting coagulation) performances in the application area? *
YesNo

2-Have you experienced any skin burns, irritation, etc. that you think were caused by the electrocautery device or plaque? *
YesNo

3-Have you experienced a situation where the cutting quality of the Electrocautery device decreased between the beginning and the end of an application? *
YesNo

4-Have you experienced a situation where the coagulation (clotting and bleeding stopping) quality of the Electrocautery device decreased between the beginning and the end of an application? *
YesNo

5-Was there any separation from the skin when you glued the patient plate during the preparation for the operation? *
YesNo

6-Did the patient plate detach from the skin during the operation? *
YesNo

7-Has there been a problem with the foot pedal becoming uncomfortable to use or wearing out? *
YesNo

8-Were there any complaints of electric shock or similar complaints from users or patients when the pedal of the device was pressed or at the time of application? *
YesNo

9-Have you encountered a situation where the alarm is not activated despite the occurrence of alarm conditions such as "Patient plaque cable disconnected from the device, plaque cable disconnected from the plaque, or patient plaque disconnected from the skin" as stated in the user manuals? *
YesNo

10-Were there any problems with the readability of the information on the screen of the electrocautery device used? *
YesNo

11-Has there ever been an application where the audible warning given during the occurrence of alarm conditions on the device and the audible warnings given when the pedal is pressed were not at a sufficient level? *
YesNo