1 5
D I R E C T H E A L T H C A R E S E R V I C E S . C O . U K
S E R V I C E M A N U A L
12. Detachable/Removable Parts
1. Mattress (Detached from the pump by removing the
CPR connector). Part No. MAT/MER/ADV/198/88/15
(or variants of for the size)
2. Electric power cable. (Removed from the pump by pulling
the cable away from the mains inlet on the side of the pump).
Part No. DHS/ADV/MLEAD
N.B. The battery is an integral part of the Rotor PCB and is not
removable or changeable.
Caution
Use of detachable parts not listed is not recommended
by Direct Healthcare Services.
13 Disposal
Please refer to DHS website for recommendations and
responsibilities for disposal within the UK WEEE guidelines.
EMI/EMC Statement and Manufacturer’s Declaration
This equipment has been tested and found to comply with the limits of EN 60601-1-2 2007.
These limits are designed to provide reasonable protection against harmful interference in both a medical and residential
environment. This equipment generates, uses and can radiate radio frequency energy and, if not used in accordance with
manufacturer’s instructions, may cause harmful interference to radio communications. However, there is no guarantee that
interference will not occur in a particular installation. If this equipment does cause harmful interference to radio or television
reception or other equipment, which can be determined by turning the equipment off and on, the user is encouraged to try to
correct the interference by one of the following measures:
®®• Reorient or relocate the receiving antenna.
• ®®Increase the separation between the equipment.
®®• Connect the equipment to an outlet on a circuit different from that to which the receiver or equipment was connected.
The equipment having been tested to operate within the limits of electromagnetic compatibility. (Immunity to interference from
nearby sources radiating radio frequency energy). Sources exceeding these limits may give rise to operation faults. Where
possible the system will sense the interference and if it is of short duration transparently take countermeasures whilst operating
near normally, or failing this will issue a warning and take measures for the continued safely of the user. Further increased levels
of energy may cause the system to stop operating, continuously generate random faults or continuous resets.
Try to ascertain the source of the interference by turning nearby or suspect equipment off, and see if the interference effects
stop. In any such event the user is encouraged to try to correct the interference by one of the following measures:
®®• Have the interfering equipment repaired or replaced.
®®• Reorient or relocate the interfering equipment.
®®• Increase the separation between the equipment and the possible source of the interference.
®®• Connect the equipment to an outlet on a circuit different from that to which the interfering equipment was connected.
Information regarding Electro Magnetic Compatibility (EMC) according to IEC60601-1-2:2007, clause 6.8
With the increased number of electronic devices such as PC’s and mobile telephones, medical devices in use may be
susceptible to electromagnetic interference from other devices.
The EMC (Electro Magnetic Compatibility) standard IEC60601-1-2 defines the levels of immunity to these electromagnetic
interferences. From the other hand, medical devices must not interfere with other devices. IEC60601-1-2 also defines the
maximum levels of emissions for these medical devices.
