Clinical Benefits - Kinetec Prima Advance CPM concept User Manual

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  • ENGLISH, page 7
INDICATIONS
• Knee replacement surgery.
• Fractures (patellar, tibia plateau, femoral,...).
• Arthrolysis.
• Hip surgery, including hip replacement, hip pinning, osteotomy,...).
• Ligament repairs.
• Arthroscopic surgery (menisectomies, patellectomies,...)
• Burns, joints sepsis,...
Bone Cancer, Warped joint surfaces, Spastic paralyses, unstable fractures, Uncontrolled infection.
The machine is not adapted for patient's height more 2 m (6'7") or under 1,40m (4'7").
1 • DESCRIPTION
KINETEC Prima Advance is a Knee PASSIVE
mobilization device enabling the extension and
flexion movement from -5° to 115°.
A - Lower limb support
B - Thigh support
C - Foot support
D - Control panel
E – Hand control
2 • ELECTRICAL CONNECTION: SAFETY FIRST.
KINETEC Prima Advance is a type B class I device.
Plug the power cord (1) on the KINETEC Prima Advance unit into a receptacle
(Voltage between 100 to 240 Vac 50/60 Hz).
IMPORTANT: Before use:
-
Check that the electrical socket is in good condition and is suitable for the splint power
supply cord. The latter complies with current standards and has a grounding socket.
-
The plug may be connected to any standard socket.
-
The socket must however have a grounded pin.
-
To connect the power supply, only use the original cable supplied with the machine.
-
Check that the cables remain free around the device so that they do not get damaged.
Fuse change
Warning: Replace the fuse with one of the same type and value: - on main socket, 2 fuses T 500 mA 250V (6.3x32)
3 • SAFETY
The physician defines the protocol and ensures that it is correctly implemented (adjustments, session duration and
frequency of use).
The patient must know the start/stop/reverse function on the control handle.
Hand control must be accessible to patient at all times. (See page 2).
KINETEC Prima Advance complies with Directive 93/42/CEE.
EXPLOSION HAZARD:
KINETEC Prima Advance is not designed for use in the presence of flammable anesthetics.
In case of electromagnetic interference with other devices move the device.
KINETEC Prima Advance is in compliance with standards in force (IEC 601.1.2), electromagnetic compatibility standard
for medical devices.
Please, do not touch the moving parts while the unit is running, pinching risk
Prima Advance
USER MANUAL
• Breaks the cycle of trauma,
inflammation and the loss of range of motion.
• Prevents joint stiffness.
• Speeds the recovery of post-operative range of motion.
• Maintains the quality of the joint surface.
• Reduces pain and oedema.
• Promotes joint cartilage healing.
• Reduces hospitalization time
• Reduces the need for pain medication.
• Provides immediate post-operative continuous passive motion.
CONTRAINDICATIONS
C
D
E
- on power supply PCB, 1 fuse F 2 A 250V (5x20)
- on PCB, 1 fuse T1.25 A (5x20))
GB

CLINICAL BENEFITS

A
1
.
B
2
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