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English
Conformity
This device complies with the requirements of the European Medical Device
Regulation (EU) 2017/745 (“MDR”).
Medical Device Classication: Class I
Manufacturer
JVC KENWOOD Corporation
3-12, Moriya-cho, Kanagawa-ku,
Yokohama-shi, Kanagawa
221-0022, JAPAN
Authorized representative
JVCKENWOOD Deutschland GmbH
Konrad-Adenauer-Allee 1-11, 61118 Vilbel, GERMANY
TEL: [phone] (German, English)
e-mail: [e-mail]
Warning
● This apparatus must be earthed because of Class I equipment.
● This apparatus is not a patient contact equipment.
● Consult your dealer about waste disposal.
● This apparatus shall not to be used in the vicinity of the patient, which is the space with
surfaces likely to be contacted by the patient or an attendant who can touch the patient.
This encloses a space within the room 1.83 m (6 feet) beyond the perimeter of the bed
in its intended location, and extending vertically 2.29 m (7-1/ 2 feet) above the oor.
● To avoid the risk of electric shock, this equipment must only be connected to a supply
mains with protective earth.
Equipment Classication
● Type of protection against electric shock: Class I equipment
● Protection against harmful ingress of water: Ordinary Equipment (IPX0)-No protection.
● Not suitable for use in the presence of ammable anesthetics or oxygen.
● Mode of operation: Continuous operation