Symbol Identification; Classifications; Disposal Of Unit - Cavitron JET Plus Instrucciones De Uso

Ocultar thumbs Ver también para JET Plus:
Tabla de contenido
Idiomas disponibles
  • ES

Idiomas disponibles

  • ESPAÑOL, página 59
SECTION 13: Specifications, continued
Footswitch
Remote Communication
Operating Environment
Transport and Storage Conditions
SECTION 14: Symbol Identification
AC POWER
TYPE B APPLIED PART EQUIPMENT
PROTECTIVE EARTH (GROUND)
Footswitch not for operating theatres
IPX1
Protection Class- IPX1
IPX1 Classification of ingress of water
Consult Instructions for Use
O/ I
AC Power Switch (0 = Off, | = On)
Footswitch
SECTION 15: Classifications
• Type of protection against electric shock:
• Degree of protection against electric shock:
• Degree of protection against the harmful ingress of water:
• Mode of operation:
• Degree of safety of application in the presence of a flammable
anaesthetic mixture with air or with oxygen or nitrous oxide:
• According to medical device directive:
SECTION 16: Disposal of Unit
U.S. - Dispose of the system components in accordance with state and local laws.
EU - Dispose of in accordance with the Waste Electrical and Electronic Equipment Directive 2002/96/EC of the European
Parliament and the Council of the European Union.
Protection Class IPX1. Not for operating theatres.
Frequency:
2405 to 2480 MHz
Power:
< 1mW
Channels:
16
Temperature: 15 to 40 Deg. Celsius (59 to 104 Deg. Fahrenheit)
Relative Humidity: 30% to 75% (non-condensing)
Temperature: -40 to 70 Deg. Celsius (-40 to 158 Deg. Fahrenheit)
Relative Humidity: 10% to 100% (non-condensing)
Atmospheric Pressure: 500 to 1060 hPa
WEEE
Class 1
Type B
Ordinary
Continuous
Equipment not suitable for use in the presence of
flammable anaesthetic or oxygen.
IIA (rule 9)
24
This symbol is a mandatory marking for devices enter-
ing the European market to indicate conformity with
the essential health and safety requirements set out in
European Directives. The symbol may be accompanied
by a four-digit identification number of the notified
body.
MEDICAL EQUIPMENT
WITH RESPECT TO ELECTRIC SHOCK, FIRE AND
MECHANICAL HAZARDS ONLY IN ACCORDANCE WITH
UL 60601-1CAN/CSA-C22.2 No. 601.1,
ANSI/AAMI ES60601-1 (2005, 3rd ed.)
CAN/CSA-C22.2 No. 60601-1 (2008),
13VA
This device complies with part 15 of the FCC Rules.
Operation is subject to the following two conditions:
1) this device may not cause harmful interference, and
2) this device must accept any interference received,
including interference that may cause undesired operation.
Foot pedal: FCC ID:TF3-DPD81861
IC: 4681B-81861
Base:
FCC ID:TF3-DPD81842
IC: 4681B-81842
Dispose of in accordance with the Waste Electrical and
Electronic Equipment Directive 2002/96/EC of the
European Parliament and the Council of the European
Union
This is a wireless device.
Tabla de contenido
loading

Tabla de contenido