认证、合规和标签
该模拟人是根据欧盟理事会指令
1999/5/EC
有关无线电及通讯终端设备
(R&TTE)
的规
定,以及欧盟理事会指令
2011/65/EU
关于
限制在电子电器设备中使用某些有害成分
(RoHS)
的指令进行
CE
标记的。
澳大利亚无线电通信和
EMC
合规标记
CANADIAN ICES-003 STATEMENT
CAN ICES-3 (B)/NMB-3(B)
制造商
制造日期
根据您所在国家的要求进行处置。
参考订单号
警告
/
注意事项符号
FCC Statement
This device complies with part 15 of the FCC rules.
Operation is subject to the following two conditions:
•
This device may not cause harmful interference
•
This device must accept any interference
received, including interference that may cause
undesired operation.
Caution
Changes or modifications not expressly approved by Laerdal Med-
ical could void the user’s authority to operate the equipment. This
equipment has been tested and found to comply with the limits
for a Class B digital device, pursuant to part 15 of the FCC Rules.
These limits are designed to provide reasonable protection against
harmful interference in a residential installation. This equipment
generates, uses and can radiate radio frequency energy and, if not
installed and used in accordance with the instructions, may cause
harmful interference to radio communications. However, there is
no guarantee that interference will not occur in a particular instal-
lation. If this equipment does cause harmful interference to radio
or television reception, which can be determined by turning the
equipment off and on, the user is encouraged to try to correct
the interference by one or more of the following measures:
•
Reorient or relocate the receiving antenna.
•
Increase the separation between the equipment and receiver.
•
Connect the equipment into an outlet on a circuit different
from that to which the receiver is connected.
•
Consult the dealer or an experienced radio/TV technician
for help.
Contains FCC ID: U3O-G2M5477
Contains FCC ID: VVXLM400
规格
Resusci Anne QCPR
、
QCPR AED
、
QCPR D
尺寸:
177
厘米
x 52
厘米
x 25
厘米
重量:
36
公斤
除颤平均为
2 x 360
焦
/
分钟,最大值(仅限
QCPR D
)
工作温度:
0
°C
至
+40
°C
湿度:
< 95%
相对湿度
存储温度:
-15
°C
至
+50
°C
通气
支持气道管理工具
下列插管装置已在气道头部进行过测试:
•
普通喉罩气道
4
•
普通喉罩气道
5
•
一次性喉罩气道
5
•
喉罩气道(快速通道)
4
•
喉罩气道(快速通道)
5
•
复合管
37 Fr
• LTS-D 4
• LTS-D 5
• Japanese Sumi NA
废物处理
模拟人含有电子元件。依照当地法规将其放置到相应的回
收地点。
欧盟指令
2012/19/EU (WEEE)
WEEE
指令:该器械是根据欧盟指令
2012/19/EU
有关废旧
电子电气设备
(WEEE)
的规定标记的。确认了该产品处置
妥当后,您就可以避免它们对环境和人体造成的潜在消极
后果;反之,如果对该产品的废弃物处置不当,就会产生
上述后果。
产品或产品附属文件上的符号表示该器械不可当作家用废
弃物来处理。而要转交到适用的收集点,进行电子和电气
设备的回收。处理时,须遵守当地的废弃物处理环保法
规。更多有关本品处理、回收和再利用的详细信息,请联
系您所在城市的办事处、您的家用废弃物处理服务部门或
您向其购买产品的挪度代表。
保修
挪度医疗
Resusci Anne QCPR / QCPR AED / QCPR D
模拟
人的保修期限为一年。请查看《挪度全球保修》了解条款
与条件。
N25270