Safety Information; Emc, Manufacturer's Declaration Of Conformity; Integrated Peristaltic Pump - Nouvag DP30 Mode D'emploi

3

Safety information

Your safety, the safety of your team and of course that of your patients is very important to us. It is
therefore essential to bear the following information in mind.
Every use of the Dispenser DP 30 different to the product description defined in chapter "Intended use and
operation", causes risks for patients and trained personnel. If physical examinations and therapies are
carried out without use of the devices then the device must be removed from the place of treatment. Avoid
any connection or close adjacency to other devices.
3.1

EMC, Manufacturer's Declaration of Conformity

The use of (RF) Radio Frequency emitting devices and equipment as well as the occurrence of negative
environmental factors in the close area of the Dispenser DP 30 may cause unexpected or adverse operation.
The connection or the placing of other devices in close vicinity is not allowed.
The Product is suitable for use in establishments of the industrial sector and hospitals. When used in the
domestic establishments, this unit may not provide adequate protection for radio services. The user must
take remedial measures such as implementation or reorientation of the product.
Use only accessories and cables as specified in the product description. Further observe the EMC
manufacturer declaration of conformity.
3.2

Integrated peristaltic pump

The integrated peristaltic pump is used for infiltration of watery solutions into the human connective tissue.
The infiltration pump is not designed for intravascular infusion of liquids.
4 Dispenser DP 30, operating instructions, REF 31678, V52/17
Dispenser DP 30