NSK iCare+ - EMC INFORMATION

iCare+ Operation Manual 10-8-1 p. 42
ENGLISH
CHAPTER 11: APPENDICES
CE Certificate of Conformity
The iCare+ device complies with the following standards:
 61010-1 and 61010-2-040 standards: Safety requirements for electrical equipment for measurement, control
and laboratory use:
 Part 1: General requirements,
 Part 2-040: Particular requirements for sterilizers and washer-disinfectors used to treat
medical materials
This product has been granted CE labeling in accordance with European directive
(EN/93/42/CE) that is applicable to laboratory and more precisely to medical devices.
The number 0535 placed under the CE label refers to the notified organism which has
validated the product's conformity and so issued the certificate of conformity.
The head office responsible for the product is the following one:
NSK WT GmbH
Portitzer Straße 69d
D-04425 Taucha
GERMANY
0535