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About this Manual

This handbook forms the Instructions for 
Use for the Keeler Cryomatic, a clinical 
instrument for cryogenic ophthalmic surgery. 
It contains complete, step-by-step instructions 
for the Cryomatic and is intended for use 
by trained medical personnel. This manual 
does not contain clinical instructions or any 
recommendations for medical applications. 
The use of the Cryomatic in any surgical 
procedure must always be at the discretion of 
a licensed medical practitioner.

About Cryomatic

The Keeler Cryomatic System and probes 
are for use in ophthalmic surgery such 
as cryopexy for retinal detachment, cyclo 
destructive procedures in refractory glaucoma, 
extraction of fragments within the vitreous 
cavity, cataract extraction, cryo destruction of 
lash follicles for trichiasis and treatment of 
retinopathy of prematurity (ROP).

Once the Cryo-Tip probe has been correctly 
positioned the freeze control is activated and 
an ice ball is formed around the tip of the 
Cryo-Tip probe and the adjacent area.

Product Description

The system comprises a control console and 
interchangeable Cryo-Tip probes which are 
connected to the console for use. The Cryo-
Tip probe is re-usable and can be sterilized by 
autoclaving or other approved methods. The 
system requires mains electricity and Nitrous 
Oxide or Carbon Dioxide gas to function, this 
is the responsibility of the user.

Console

The Cryomatic console is a self contained 
system. The console provides the connection 
points for the Cryo-Tip probe, footswitch, 
mains electricity, gas supply and scavenging 
system. Freeze cycles are controlled by the 
user operating the footswitch. When the 
footswitch is depressed the Cryo-Tip probe 
freezes and when the footswitch is released 
the Cryo-Tip probe defrosts. Routine functions, 
like purging the Cryo-Tip probe are performed 
automatically when the Cryo-Tip probe is 
connected to the system.

Cryo-Tip Probes

The Cryo-Tip probe is connected to the 
Cryomatic console via a simple quick release 
coupling. The system will not operate until 
this connection is correctly made. Each Cryo-
Tip probe is a complete assembly and no 
attempt should be made to dismantle or 
separate the coupling from the probe.

When the footswitch is pressed, high pressure 
cryogen gas is circulated through the Cryo-
Tip probe, rapid gas expansion in the probe 
tip causes freezing according to the Joule-
Thompson principle. The freezing zone of 
the Cryo-Tip probe is limited so that the ice-
ball propagates only at the tip. When the 
footswitch is released, an active de-frost is 
caused by the equalisation of pressure on 
either side of the Joule-Thompson nozzle.  
The gas condenses releasing its latent heat 
causing a rapid de-frost.

The Cryo-Tip probe assembly is re-usable and 
as such is fully autoclaveable according to the 
procedures outlined in this manual.

2. Introduction

Содержание Cryomatic

Страница 1: ...Next Home Back 1 Keeler Instructions for use...

Страница 2: ...ons End of Use 6 Cryo Tip Probes 7 Cleaning Sterilisation Cleaning Steam Sterilisation Cleaning the Console 8 Servicing and Preventative Maintenance Scheduled Maintenance User Maintenance 9 Spare Part...

Страница 3: ...unity Relevant accessories are listed in the Spare Parts Accessories section For your own safety and the safety of the equipment always take the following precautions Keep the console away from source...

Страница 4: ...on Dioxide gas to function this is the responsibility of the user Console The Cryomatic console is a self contained system The console provides the connection points for the Cryo Tip probe footswitch...

Страница 5: ...as cylinder status and freeze timer 3 Footswitch Connection Connection point for footswitch plug 4 Cryo Tip Probe Interface Pneumatic and electrical connections for probe 5 Electrical Input IEC connec...

Страница 6: ...the footswitch to the appropriate connection point on the rear of the console noting the alignment of the orientation key see page 5 The footswitch can be disconnected for storage and to facilitate c...

Страница 7: ...e with ISO R 32 and ANSI NFPA 99 USA Ensure there is enough gas in the Cylinder prior to starting the procedure The console Cylinder Symbol indicates empty when the gas supply pressure drops below 350...

Страница 8: ...tion protocol before using a Cryo Tip probe Allow Cryo Tip probe to cool to room temperature after a sterilization procedure Before connecting the Cryo Tip probe inspect it for signs of obvious damage...

Страница 9: ...ure for the probe The pulsing may vary or cease completely depending on the pressure of gas in the cylinder If the probe performance drops below 100 permanently check the cylinder gas pressure or susp...

Страница 10: ...ns The Cryomatic system has the ability to detect a range of system faults In the unlikely event of a fault condition arising the fault symbol icon will flash and a short error message will be display...

Страница 11: ...rd Range Part No Description 2509 P 8000 2 5mm Standard Retinal Probe 2509 P 8001 2 5mm Extended Retinal Probe Special Range 2509 P 8002 2 5mm Mid Reach Retinal Probe 2509 P 8005 3mm Glaucoma 2509 P 8...

Страница 12: ...e Cryo Tip probe Instructions Point Of Use No particular requirements although excess soiling can be removed with disposable cloth paper wipe Containment Transportation Care should be taken to ensure...

Страница 13: ...ed When sterilising multiple probes in one sterilization cycle ensure that the manufacturer s maximum load is not exceeded Table 1 sterilizer type temperature pressure exposure time drying time pre va...

Страница 14: ...abrasive metal polish should be used b Cleaning the console surface c Inspecting the Cryo Tip probes for signs of damage before every use d Inspecting the footswitch and cord for signs of damage befor...

Страница 15: ...ptor N2 O Size VF 2508 P 7016 Cylinder Adaptor CO2 Size VF 2509 P 8009 Cylinder Adaptor N2 O US CGA326 2509 P 8012 Instructions For Use 2509 P 8011 High Pressure Hose 1m 2509 P 8014 High Pressure Hose...

Страница 16: ...contact supplier for repair Probe freezes but performance is poor Possible partial blockage in the probe possibly caused by excess moisture after sterilisation procedure Probe may appear to begin to...

Страница 17: ...in this warranty are expressly conditional upon the following i No alterations or repairs of any malfunction of the system shall be made to the system except by the manufacturer or his authorized repr...

Страница 18: ...Weight 2 5kg 6lbs Environmental Conditions Storage Operating Temperature Range 20 C to 50 C 10 C to 40 C Relative Humidity 10 to 80 30 to 70 Atmospheric Pressure 500hPa to 1060hPa 700hPa to 1060hPa Cl...

Страница 19: ...symbol contains an activity bar whenever the gas supply is being checked It is solid when reporting cylinder pressure Ready Symbol Displayed whenever the freeze function can be activated via the foot...

Страница 20: ...c System uses RF energy only for its internal function Therefore its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment RF emissions CISPR 11 Class B...

Страница 21: ...rcial or hospital environment Surge IEC 61000 4 5 1kV differential mode 2kV common mode Mains power quality should be that of a typical commercial or hospital environment Voltage dips short interrupti...

Страница 22: ...ed by an electromagnetic site surveya should be less than the compliance level in each frequency rangeb Interference may occur in the vicinity of equipment marked with this symbol NOTE 1 At 80MHz and...

Страница 23: ...P 800MHz to 2 5GHz d 2 3 P 0 01 0 12 0 12 0 23 0 1 0 38 0 38 0 73 1 1 2 1 2 2 3 10 3 8 3 8 7 3 100 12 12 23 For transmitters rated at maximum output power not listed above the recommended separation...

Страница 24: ...of continued product improvement we reserve the right to alter specifications at any time without prior notice Keeler Instruments Inc 456 Parkway Broomall PA 19008 USA Toll Free 1 800 523 5620 Tel 610...

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