59
R5913170 /00
MDFC-8232
E346057
Indicates the device is approved according to the UL Recognition regulations.
E346057
MEDICAL
–
GENERAL MEDICAL EQUIPMENT
AS TO ELECTRICAL SHOCK, FIRE AND MECHANICAL HAZARDS ONLY
IN ACCORDANCE WITH ANSI/AAMI AS60601-1:2005/(R)2012, CSA CAN/CSA-C22.2
NO. 60601-1:14
E346057
Indicates the device is approved according to the UL regulations for Canada and US.
Indicates the device is approved according to the UL Demko regulations.
Indicates the device is approved according to the CCC regulations.
Indicates the device is approved according to the VCCI regulations.
Indicates the device is approved according to the KC regulations.
Indicates the device is approved according to the BSMI regulations.
Indicates the device is approved according to the PSE regulations.
Indicates the device is approved according to the RCM regulations.
Indicates the device is approved according to the EAC regulations.
Caution: Federal law (United Stated of America) restricts this device to sale by or on the
order of a licensed healthcare practitioner.
IS 13252 (Part 1)
IEC 60950-1
R-xxxxxxxx
www.bis.gov.in
Indicates the device is approved according to the BIS regulations.
Indicates the device is approved according to the INMETRO regulations.
Содержание MDFC-8232 3HB
Страница 6: ...R5913170 00 MDFC 8232 6...
Страница 7: ...7 R5913170 00 MDFC 8232 Welcome 1...
Страница 10: ...R5913170 00 MDFC 8232 10 Welcome...
Страница 11: ...11 R5913170 00 MDFC 8232 Parts controls and connectors 2...
Страница 17: ...17 R5913170 00 MDFC 8232 Display installation 3...
Страница 23: ...23 R5913170 00 MDFC 8232 Daily operation 4...
Страница 28: ...R5913170 00 MDFC 8232 28 Daily operation...
Страница 45: ...45 R5913170 00 MDFC 8232 Troubleshooting 6...
Страница 47: ...47 R5913170 00 MDFC 8232 Important information 7...
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