Leica M205 FA Leica EL6000 Safety Notes, General safety notes, Rights to any warranty claims

Leica EL6000 – Safety Notes

•The manufacturer assumes no respon- sibility or liability for any use outside of

the intended use or use outside of the specifica- tions from Leica Microsystems Wetzlar GmbH or any risks resulting from such use.

In such cases, the Declaration of Conformity shall be invalid.

•This (IVD) device is not intended for use in the patient environment defined by

DIN VDE 0100-710. It is also not intended to be combined with medical devices as defined by EN 60601-1. If a microscope is electrically connected to a medical instrument in accor- dance with EN 60601-1, the requirements defined in EN 60601-1-1 shall apply.

General safety notes

This safety class 1 device was built and tested in accordance with

EN 61010-2-101:2002 EN 61010-1:2001, IEC 1010-1:2001,

Safety requirements for electrical equipment for measurement, control and laboratory use.

The devices and accessories described in this operating manual have been tested for safety and potential hazards.

The responsible Leica affiliate or the main plant in Wetzlar must be consulted whenever the device is altered, modified or used in conjunc- tion with non-Leica components that are outside of the scope of this manual.

•Unauthorized alterations to the instru- ment or noncompliant use shall void all

rights to any warranty claims.

•If any safety defects or malfunctions of the Leica EL6000 are identified, the

instrument must be immediately disconnected from the power system and secured against additional use. For repair, the Leica EL6000 must be sent to the supplier or an authorized representative of the supplier.

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