What to do if Braun Aesculap GN060 shows error code F1?
If your Braun Medical Equipment displays error code F1, it means that several buttons were activated simultaneously, or an object is pressing on multiple buttons. Make sure to only press one button at a time, or remove any objects from the keyboard. If the error persists, it likely indicates a keyboard defect.
What to do if Braun Aesculap GN060 Medical Equipment shows error code F2?
If your Braun Medical Equipment displays error code F2, it means that a key has been activated for longer than 15 seconds or an object is pressing on the keyboard. Try activating the keys for a shorter period, or remove any obstructing objects from the keyboard. If the error continues, it suggests a potential keyboard defect.
What to do if Braun Medical Equipment shows error code F4?
If your Braun Medical Equipment displays error code F4, it indicates that it was not possible to write to the EEPROM. Try switching the HF device off and then on again. If the error message continues to appear, it indicates an error in the EEPROM.
What to do if Braun Aesculap GN060 Medical Equipment shows error code F5?
If your Braun Medical Equipment displays error code F5, which means it was not possible to read the EEPROM, follow the steps for error code F4: switch the HF device off and then on again. If the error message continues to appear, it indicates an error in the EEPROM.
What to do if Braun Aesculap GN060 shows error code E1-E6?
If your Braun Medical Equipment displays error codes E1 through E6, switch off the HF device and switch it on again. If the error message continues to be displayed, there is a device error.
What to do if Braun Aesculap GN060 Medical Equipment shows error code F3?
If your Braun Medical Equipment displays error code F3, release the foot switch and activate it again. If the error message continues to be displayed even if the foot switch is not activated, it is possible that the foot switch or the lead cable of the foot switch is defective.
Explains the function of various buttons and displays on the device's front panel.
Details symbols used on the product and its packaging for identification.
Lists the main sections and their corresponding page numbers for document navigation.
Covers general handling safety, including legal restrictions and operational warnings.
Details safety compliance with IEC regulations and the risk of electric shock.
Highlights critical warnings regarding patient injury from device faults, burns, and stimulation.
Details product scope, required components, and approved medical applications.
Explains the device's operating principle and provides performance data charts.
Covers accessory safety, first-use instructions, and system setup warnings.
Provides instructions on how to securely stack accessory devices onto the HF unit.
Details unit handling, dismantling, and critical voltage setting procedures.
Guides on connecting the device to power and accessories for system setup.
Highlights safety risks related to connecting instruments and potential life-threatening situations.
Outlines essential function checks required before operating the device.
Covers general safety warnings during device operation, including visual control.
Explains how to operate controls like switching on, mode selection, and dosage adjustment.
Details how to store device settings and retrieve them later.
Covers activating HF output, taking the device out of service, and error handling.
Explains protection mechanisms against faulty operation like key presses and permanent activation.
Details internal monitoring systems for dosage accuracy and error prevention.
Covers the validated reprocessing procedure and general safety instructions.
Provides general information and preparation steps for cleaning and disinfection.
Details safety precautions and methods for cleaning and disinfecting the device.
Covers wipe disinfection procedures and inspection of the device.
Details maintenance, checks, and safety considerations for storage and transport.
Outlines maintenance requirements and the annual safety inspection process.
Describes the protocol for documenting safety inspection findings and measurements.
Lists error codes, their detection, causes, and recommended remedies for troubleshooting.
Details the fuse replacement procedure and associated electrical safety warnings.
Provides contact information for technical service, repairs, and support.
Lists accessories, spare parts, and the device's classification according to directives.
Details electrical, mechanical, and EMC specifications of the HF surgical device.
Covers applied part details, EMC compliance, and conforming standards.
Specifies ambient conditions for device operation and transport.
Provides information and guidance on proper product disposal and relevant regulations.
Provides contact details for the US distributor and Canadian product information inquiries.
General| Brand | Braun |
|---|---|
| Model | Aesculap GN060 |
| Category | Medical Equipment |
| Language | English |
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