36/107 Rev. 12 / 12.2022 AB2200DEENFRIT
1 Use according to specification
The centrifuge MIKRO 220 / MIKRO 220 R is an in vitro diagnostic medical device according to the ln Vitro
Diagnostic Medical Devices Regulation (EU) 2017/746.
The device is used for centrifuging and enriching sample material of human origin for subsequent further processing
for diagnostic purposes. The user can set each of the variable physical parameters within the limits set by the device.
The centrifuge may only be used by qualified personnel in closed laboratories. The centrifuge is only intended for the
use referred to above. Intended use also includes observing all instructions in the Operating Manual and compliance
with the required inspection and maintenance work.
Any other use or use beyond this is considered improper. Andreas Hettich GmbH & Co. KG shall not be liable for any
damage arising from this.
2 Remaining risks
The device is built according to the state-of-the-art and the recognized safety regulations. If used and handled
improperly, there could be life-threatening danger to the user or third parties, or the device could be impaired or there
could be other property damage. The device is only to be used for its intended purpose and only when it is in safe
working condition.
Malfunctions which could affect safety must be corrected immediately.
3 Technical specifications
Maximum relative humidity 80% for temperatures up to 31°C, linearly
decreasing to 50% relative humidity at 40°C.
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