Removing The Sterile Material - MELAG Vacuclave 550 Manual De Uso

If automatic log output after the end of the program is activated in the menu (= immediate output), the log of the run pro-
gram is output to the activated output media after the door is opened.
Approval process
According to RKI "Hygiene requirements for the treatment of medical products", instrument reprocessing ends with the
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documented approval for storage and application of the
tion and batch approval and must be performed by authorised and expert personnel.
Batch approval comprises the checking of the process parameters using the sterilization results on the device and the
sterilization log as well as checking of the individual packaging for damage and residual moisture. The sterilization log re-
cords the approval of the
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the sterile material requires the user PIN of the person who provides approval for the batch and the indicators.
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See also:
▪ Logging [} page 35]
▪ Administrative settings [} page 46]

Removing the sterile material

CAUTION
Danger of burns from hot loads
Use a tray lifter or heat protection gloves.
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CAUTION
Unsterile instruments resulting from damaged or burst packaging. This endangers the health of your
patients and practice team.
Should the packaging be damaged or have burst after sterilization, wrap the load again and re-sterilize it.
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Comply with the following specifications when removing the sterile material:
Never use force to open the door. This could damage the device or result in the emission of hot steam.
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Hold the mount level when removing it from the device. Otherwise, the load could slide off.
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Hold the tray level when removing it from the steam sterilizer. Otherwise, the load could slide off.
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When removing the load from the device separately, ensure that the mount does not slide out unintended.
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Use a tray lifter or suitable protective gloves to remove the tray.
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Use both hands and two tray lifters to remove large or long trays.
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Never touch the sterile material, the sterilization chamber, the mount or the inside of the door with bare hands. The
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components are hot.
Check the packaging of the sterilized equipment for damage when removing it from the device. Should the
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packaging be damaged, re-pack the load and re-sterilize it.
batch and any indicators. Depending on the setting in the user administration, approval for
sterile material. The approval process consists of
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8 Sterilization
batch indica-
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