Pereg GmbH offers a special range of indicators and test methods for washer-disinfectors, ultrasonic cleaners, and manual cleaning procedures.
In 1997 we asked ourselves: How can one neglect the most important step when reprocessing surgical instruments? If it’s not clean, it can’t be sterile was a common phrase but there was not much standardisation, quality assurance, or enough science behind cleaning processes.
Now PEREG GmbH is the leading company for cleaning monitoring when reprocessing surgical instruments. This was achieved by believing in the importance of cleaning and knowing the science behind it. In cleaning we do not use standardised parameters as in sterilisation, therefore monitoring a cleaning process needs to be achieved in a different way: Tests for cleaning efficacy must be adapted to the practical situation.
A test soil correlating to blood is one important step but blood behaves differently in various cases such as being cleaned from an ordinary steel surface compared to cleaning the inside of an instrument. Also blood residues after an inefficient cleaning process do not have much in common anymore with fresh blood. We took these important factors into consideration and developed a special range of indicators and test methods for washer-disinfectors, ultrasonic cleaners and manual cleaning procedures:
TOSI
Routine monitoring and validation of cleaning efficacy according to EN ISO 15883
TOSI test objects are simulated transparent surgical instruments. The contamination is correlating to the practical situation. If a cleaning process cannot clean the TOSI it is not efficient enough to clean blood contaminated instruments! The TOSI will not only give a yes/no answer for blood cleaning efficacy but will also give feedback regarding the cause of a problem. Note: Contaminated instruments are a hygiene risk and need to be rejected. Instruments need to be free of any residue!
Routine monitoring and validation of cleaning efficacy.
ENDOSCOPE WASHERS NEED TO BE REGULARLY MONITORED
The FlexiCheck-system is a unique product for monitoring the cleaning efficiency of the Flexible Endoscope washer. Flexible Endoscopes are often contaminated with mucus however blood is also a possible contaminant. FlexiCheck will monitor the efficiency of the washer and the detergent. TOSI-FlexiCheck combines 2 different test soils on one test strip: One is the standardised blood test soil and the second is a polysaccharide mixture. For reprocessing Flexible Endoscopes washers with channel irrigation systems are recommended. FlexiCheck is connected to this system and will simulate a single channel at one time.
2 COMMON WAYS TO CLEAN CANNULATED INSTRUMENTS
Routine Monitoring and Validation of cleaning efficacy for Cannulated instruments according to EN ISO 15883
Test Kit for detection of blood-protein residue on surgical instruments. Test method according to EN ISO 15883. For routine monitoring and validation of cleaning efficacy.
HemoCheck-S is based on an enzymatic reaction also used in forensic science. Blood contains large quantity of peroxidases and can be detected in very small quantity. Detects insoluble blood-protein residue. Different than standard protein testing HemoCheck-S gives a 100% clear answer by blood being the best marker for a hygiene risk! A colour change to blue-green on the swab indicates blood-protein residue on the tested area. NOTE: Contaminated instruments are a hygiene risk and need to be rejected. Instruments need to be free of any residue.
Test for residual water in Flexible Endoscopes
HydroCheck-E can detect a very small amount of residual water inside an endoscope channel to avoid recontamination during storage. A swab is used to sample any residual water from the endoscope channel and is then tested with the HydroCheck-E. A purple spot on the swab indicates residual water in the tested channel. Large amount of residual water will turn the swab completely purple. NOTE: Residual water in endoscopes is a hygiene risk to patients. Moisture allows microorganisms to survive and multiply. Endoscopes need to be completely dry before storage.
Monitoring the energy of ultrasonic bath for cleaning of surgical instruments Routine monitoring and validation according to AS/NZS 4187.
The process of ultrasonic cleaning relies upon the occurrence of cavitation. This effect will trigger a chemical reaction in the SonoCheck changing its colour. SonoCheck is used to monitor the ultrasonic energy level during the cleaning of surgical instruments. SonoCheck is also used to measure the performance of the individual transducers during the functional test. When the ultrasonic cleaner is supplying sufficient energy, SonoCheck will show a positive result within the recommended cycle time. Effects such as insufficient energy, overloading, water level and de-gassing will increase the time needed for the colour change. In the case of a major problem SonoCheck will not change at all.
Highly absorbent cleaning and monitoring brushes for Flexible Endoscopes.
Endoswabs are based on a highly absorbent polyester fibre manufactured into a flexible Endoscope cleaning brush. Endoswabs will absorb and collect residue out of the channel, while nylon fibres glide through mucus residue inside the channel. Endoswabs are used for the manual cleaning step according to the flexible Endoscope cleaning procedure. Available in 4 sizes, for use in 1.5 – 5.0mm flexible Endoscopes channels. NOTE: Contaminated instruments are a hygiene risk and need to be rejected. Instruments need to be free of any residue!
Detection of protein residue on instruments and surfaces. For routine monitoring and validation of the cleaning efficacy.
Pyromol-Test is based on a dye binding method which is also used in clinical chemistry. Blood contains large amount of protein which can be detected at a low level. The Pyromol-Test is used for the detection of protein residue where HemoCheck-S cannot be used. Example: Other sources of protein than blood. A blue spot on the swab indicates protein residue on the tested surface. NOTE: Contaminated instruments are a hygiene risk and need to be rejected. Instruments need to be free of any residue!
Detection of protein residue in Endoscope Channels. For routine monitoring and validation of the cleaning efficacy.
Pyromol-Test is based on a dye binding method which is also used in clinical chemistry. Contamination in an endoscope contains protein which can be detected at a low level. Pyromol-E will detect protein residue after manual or automated reprocessing. A blue spot on the swab indicates protein residue in the tested channel. NOTE: Contaminated instruments are a hygiene risk and need to be rejected. Instruments need to be free of any residue!
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For more information on our Pereg GmbH range please contact our friendly Customer Care staff on 1300 552 003 or at care@invitro.com.au