PARAMOUNT BED cococia Fuka, Instruction Manual

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SPECIFICATIONS
25

Air m attress and pump
Product name Air Mattress cococia Fūka
Model No.
KE - 951E
KE - 951E2
KE - 951E3
KE - 953E
KE - 953E2
KE - 953E3
KE -961 E
KE -961 E2
KE -961 E3
KE -963 E
KE -963 E2
KE -963 E3
KE -958 E
KE -958 E2
KE -958 E3
KE -959 E
KE -959 E2
KE -959 E3
KE -968 E
KE -968 E2
KE -968 E3
KE -969 E
KE -969 E2
KE -969 E3
Type of protection for electrical shock Class I device
Level of protection for electrical shock Type BF applied part
Protection code IEC 60529 IP21
Air mattress
Size (cm)
Width 91 83 91 83 86 91 86 91
Length 191 200
Thickness 13 15 13 15
Material
Top cover
Polyurethane, polyester
(antibacterial, flame - resistant, and waterproof)
Bottom cover
Polyvinyl chloride, polyester
(antibacterial, flame - resistant, and waterproof)
Blowing tube PVC
Air cell Nylon, polyurethane
Coupling PBT resin
Number of air cells 17 18
Product weight (kg) 4.5 4.3 6.6 6.3 4.4 4.5 6.5 6.7
Pump
Size (cm)
Width 25
Depth 11
Height 22
M aterial Case ABS resin (flame - resistant, chemical - resistant)
Power
supply
Plu g 2P
Length 4.6 m
Product weight (kg) 2.2
Guaranteed
conditions
O perating temperature/
humidity/air pressure
15 to 40°C / 30 to 75% RH / 800 hPa to 1060 hPa /
Operational altitude ≤ 2 000 m
Storage temperature/
humidity/air pressure
5 to 60° C / 30 to 85 % RH / 800 hPa to 1060 hPa
User's weight (kg) 30 to 180
Power supply voltage / frequency AC 100 - 240 V 50/60 Hz
Max current
0.2 A-0.1 A
Main fuse 1 A / 250 V
Service life 2 years (based on Paramount Bed data), excluding consumable items.

Basic performance
Function for supporting the user’s body weight .

Frequently used functions
Hardness adjustment and alternate pressure function .

Applicable standards
The air mattress described in this instruction manual is designed and manufactured according to the following
standards.
Applicable standards : IEC60601 - 1: 2012+CORR.1: 2014
: IEC60601 -1-2: 2014
: IEC60601 -1-11: 2015
: EN60601 - 1: 2006+A1:2013
: EN60601 -1-2: 2015
: EN60601 -1-11: 2015
Classification as medical device in Europe : Class I