In accordance with IEC 60601-2-52:2009, "Particular requirements for the safety and essential per-
formance of medical beds", the following standards are used:
IEC60601-2-52, Section 201.6.2
Protection against electrical shock: Protection class
II
IEC60601-2-52, Section 201.6.3
Control panel symbols (depending on model, cus-
tomer requirements)
IEC60601-2-52, Section 201.8.11.3.2
Power supply lead: only >= 2.5 m length
Power supply lead: for example, EPR or similar
IEC60601-2-52, Section 201.9.2.2.5
Continuous operations: Control unit only with button
IEC60601-2-52, Section 201.9.2.3.1
Unintentional movement:
Prevented by means of a locking mechanism (such
as Control box, Supervisor, IPROXX
®
SE,
IPROXX
®
, or Meditouch)
IEC60601-2-52, Section 201.9.6.2.1
Noise level: <=65dB(A) (refer to EN60601-2-38)
IEC60601-2-52, Section 201.11.1.1
Temperatures
IEC60601-2-52, Section 201.11.6.5.101
Protection against water ingress: only for >= IPX4
IEC60601-2-52, Section 201.11.8
Power outage:
for example, battery usage, depending on version
(customer requirement)
IEC60601-2-52, Section 201.13.1.4
Special mechanical hazards:
Prevented by means of a locking mechanism (such
as Control box, Supervisor, IPROXX
®
SE,
IPROXX
®
, or Meditouch)
IEC60601-2-52, Section 201.15.3.4.1
Mechanical attachment – handset
IEC60601-2-52, Section 201.15.4.4
Displays: Ready indicator is not required
IEC60601-2-52, Section 201.17
Electromagnetic compatibility
IEC60601-2-52, Section BB.3.3.3
Dimensions: vary according to the model (customer
requirement)
IEC60601-2-52, Section BB.3.4.1
Operating forces
