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7 • Cleaning and disinfection
80113-401_V24023
2023-05
2. Or use ready-for-use cleaning wipes with a cleaning agent solution.
3. Clean all visible contamination (e.g., blood) off the surfaces. Residual contamina-
tion may reduce the effectiveness of the subsequent disinfection.
4. Visually inspect all surfaces after cleaning. If you find any residual contamination,
repeat cleaning until all contamination has been removed.
Note: If you cannot carry out a full clean, do not carry out a wipe disinfection. Do not
use the unit or the cart. Contact Technical Service.
Disinfection
Use only disinfectants that comply with relevant national standards. Comply with the
manufacturer’s specifications for the disinfectant, particularly regarding material com
-
patibility. If you use different products for cleaning and disinfection, the products must
be compatible with each other.
1. Mix the disinfectant in a concentration specified by the manufacturer. Moisten
low-lint single-use wipes with the disinfectant solution.
2. Or use ready-for-use disinfectant wipes with a disinfectant solution.
3. Wipe the surfaces thoroughly.
4. Ensure that the surfaces are completely wetted.
5. Leave the disinfectant to work as specified by the manufacturer (exposure time).
6. Keep the surfaces wet throughout the entire exposure time.
7. Visually inspect the surfaces for any damage after disinfection.
Note: If the surfaces are damaged, do not use the unit or the cart. Contact Technical
Service.
Validated procedure for cleaning and disinfection
Cleaning
Clean with mikrozid universal wipes premium, Schülke & Mayr GmbH, Norderstedt,
Germany. Clean all visible contamination (e.g., blood) off the surfaces. Residual con
-
tamination may reduce the effectiveness of the subsequent disinfection.
Disinfection
Disinfect with mikrozid universal wipes premium, Schülke & Mayr GmbH, Norderstedt,
Germany. Leave the disinfection solution to work for one minute, making sure it is vis
-
ibly wetted.
Erbe recommends this processing procedure. Other equivalent procedures are possi-
ble. The user must ensure that the procedures used are suitable by means of suitable
measures (e.g., validation, routine monitoring, check of material compatibility).
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