EN
6/38
Rev. 02 / 11.2022
AB1203EN_SA
3 Intended
use
This device is a medical product (laboratory centrifuge) according to the in vitro diagnostic medical devices regulation
(EU) 2017/746.
The centrifuge was designed only for the separation of materials or mixtures with a density of no more than 1.2
kg/dm³.
This includes sample preparations for molecular biological investigations in the clinical area. Here, centrifugation is a
decisive step for extracting and purifying DNA and RNA from patient samples. In addition, many special kits are used
routinely. If kits and spin columns are used, the centrifuge, with a sufficiently high centrifugal acceleration and its
specially designed rotor for the centrifugation of spin column kits, meets the requirements for sample preparation in
infection diagnostics.
The centrifuge is only meant for this purpose.
Another use or one which goes beyond this, is considered to be non-intended. The company Andreas Hettich GmbH
& Co. KG is not liable for damage resulting from this.
Observing all information in the operating instructions and complying with the measures described therein is also a
part of the intended use.
If the centrifuge is installed in another device or in a system, the manufacturer of the overall system is responsible for
its safety.
4 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.
