RFID) emit electromagnetic radiation, the function of the product may be impaired. High-
frequency communication equipment can affect electrical medical products and impair their
performance.
Observe the information on electromagnetic compatibility, see chapter Electromagnetic
compatibility [p. 53].
The discharge of a defibrillator can cause image loss.
If the image has not recovered after 4 seconds, switch the camera control unit off and on
again.
3.8 Product not clean
The product is not clean when delivered. The use of products that have not been cleaned
poses a risk of infection for patients, users, and third parties.
Reprocess the product in line with the reprocessing instructions before initial use and
every subsequent use.
3.9 Failure of products
The product may fail during use.
Perform an equipment test before use, see chapter Preparation [p. 24].
If the image fails during the procedure, remove the camera from the endoscope and
continue the procedure optically.
If the surgery cannot be continued optically, determination of how to further the procedure
is at the physician's discretion based on the surgical circumstances.
Have a replacement system ready for each application.
Instructions for use • IMAGE1 S • 705LZA_EN_V2.1_05-2022_IFU_FDA
Safety and warning
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