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Guidelines for the control of sterilization using sterilization indicators IS-120, IS-132, IS-160, IS-180 of the Scientific-Production Company "VINAR"


APPROVED Head of Prevention Department of the Ministry
R.I. Khalitov
Healthcare of the Russian Federation
11.06.93 №11-8 / 03-54
General provisions
These Guidelines are intended
for all health care workers who perform work related to the decontamination and sterilization of medical instruments and medical devices, as well as using sterile medical instruments and medical devices in their activities.
Indicators of sterilization of the production of APF “VINAR” are a means of monitoring the sterilization regimes, which exclude the possibility of using instruments and materials sterilized in defective or improperly operated devices in the examination and treatment of patients. Indicators allow you to determine not only the temperature that was achieved during the sterilization process, but also the time of its impact on the objects to be sterilized.
Indicators IS-120 and IS-132 are designed for simultaneous control in steam sterilizers according to GOST 19569-80 of the temperature and time of sterilization of medical equipment, as well as the presence of steam during sterilization. The IS-120 indicator is used for the sterilization mode: temperature 120 + 2 ° С (vapor pressure 0.11 + + 0.02 MPa) for 45 + 3 min, indicator ИС-132 - temperature 132 ± 2 ° С (vapor pressure 0 , 20 + 0.02 MPa) during 20 + 2 min.
Indicators IS-160 and IS-180 are designed for simultaneous control in air sterilizers in accordance with GOST 22649-83 of the temperature and time of sterilization of medical equipment products. Indicator IS-160 is used for sterilization mode: temperature 160 ± 3 ° С during 150 + 5 min, IC-180 indicator - temperature 180 + 3 ° С during 60 + 5 min.
The indicator is a strip of paper, on one side of which an indicator layer is applied, Changing its color to the color of the reference, while observing the sterilization regime. NPF "VINAR" also manufactures sterilization indicators, on the second side of which an adhesive layer is applied. The standard is a strip of paper, one side of which is painted in color, with which the indicator color must match with respect to the sterilization regime.
1.6. Indicators are manufactured in accordance with TU 480153-001-92 (agreed with the Ministry of Health of the Russian Federation on June 10, 1993).
The use of indicators
To control sterilization regimes with different temperature parameters, an appropriate sterilization indicator should be used.
Method
sterilization
Sterilization mode parameters Type of
indicator
temperature
sterilization
sterilization exposure (min)
Air method 160 150 IS-160
Air method 160 60 IS-180
Steam method 120 45 IS-120
Steam method 132 20 IS-132


Sterilization is considered effective if the color of all indicators embedded in the sterilizer chamber corresponds to the color of the standard or is darker than the standard.

The color of the indicator is lighter than the reference at any point in the sterilizer indicates ineffective sterilization.
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Guidelines for the control of sterilization using sterilization indicators IS-120, IS-132, IS-160, IS-180 of the Scientific-Production Company "VINAR"

  1. Instruction No. 154.021.98 PI on the use of single-use sterilization indicators IS-120, IS-132, IS-160, IS-180 for monitoring the parameters of operating modes of steam and air sterilizers
    AGREED NIIID Director Academician of the Russian Academy of Medical Sciences MG Shandala, 01/07/99. APPROVED: Head of the Department of State Sanitary and Epidemiological Surveillance of the Ministry of Health of Russia A.A. Monisov 07/18/99. control parameters parameters (temperature, time) of steam and air sterilizers. The use of indicators allows you to detect non-compliance with the sterilization regime, due to technical failure of sterilizers,
  2. Guidelines for the sterilization of ligature suture material in medical institutions
    (Approved by the Main Epidemiological Directorate of the Ministry of Health of the USSR of July 19, 90 No. 15-6 / 34) General Provisions The methodological recommendations were drawn up in accordance with OST 42-21-2-85 “Sterilization and disinfection of medical products. Methods, means and modes. Methodical recommendations are intended for the staff of medical institutions that are engaged in the preparation of ligature
  3. Guidelines for the use of deoxon-1 for disinfection and sterilization
    (Approved by O. Imamaliev, Deputy Head of the General Directorate for Quarantine Infections, USSR Ministry of Health, December 24, 80 Xa 28-15 / 6) General provisions Dezokson-1 is a colorless liquid with a specific smell of vinegar. Contains in its composition 5.0-8.0% peracetic acid. The drug is highly soluble in water, alcohol and other solvents. Solutions of deoxon-1 corrode products from low-grade
  4. On approval of guidelines for cleaning / disinfection and sterilization of endoscopes and tools for them used in medical institutions
    ORDER of the Ministry of Health of the Russian Federation of 16. Ob-97 No. 184 In order to improve and streamline the processing of devices and tools used in departments, departments, and offices of endoscopy, I order: To put in place the "Guidelines for cleaning, disinfecting and sterilizing endoscopes and tools for them used in medical institutions ”(Appendix). Executives
  5. Guidelines for the use of deoxon-4 for disinfection and sterilization
    (Approved by the Head of the State Committee for Sanitary and Epidemiological Surveillance of the Russian Federation, V. I. Chiburayev, No. 11-114 / 3323-1 of June 29, 1992). Designed for workers of disinfection stations, deserts of territorial centers of the State Sanitary and Epidemiological Surveillance, and medical institutions. General information Dezokson-4 is a colorless liquid with a specific smell of vinegar. Contains in its composition 5-9%
  6. Requirements for the organization of control over disinfection and sterilization in hospitals
    (Approved by Order M3 of the USSR of 03.09.91 No. 254) Quality indicators The control of disinfection and sterilization measures in medical institutions is carried out by sanitary-epidemiological and disinfection stations simultaneously with the control of the sanitary-anti-epidemic regime. Control is carried out: visually, by bacteriological and chemical methods, as well as with
  7. Guidelines for the use of the drug "Gigasept FF" for disinfection and sterilization of medical products (the company "Schülke and Mayer GMBH", Germany)
    (Approved by the Head of the State Sanitary and Epidemiological Surveillance of the Russian Federation on August 31, 1992) Intended for the medical staff of medical institutions and employees of disinfection stations and territorial centers of the State Sanitary and Epidemiological Surveillance. 1. General information "Gigasept FF" manufactured by Schülke and Meyer (Germany) is a composition containing as
  8. Disinfection and sterilization preparations permitted for use in hospitals
    Designation of Processed Items: - Tools, Equipment, surfaces, dishes, linens. - Endoscopes, optics, thermolabile products. - Dental instrument. - Hands, skin and mucous membranes. 80 "src =" / files / uch_group35 / uch_pgroup38 / uch_uch1035 / image / 96.gif "> In recent years, domestic low-cost and high-performance equipment has become more and more common for processing premises and sanitary equipment.
  9. Sterilization
    In the scope of EN standards, the use of sterile instruments on or in a patient assumes that the instruments are properly cleaned and disinfected, sterilized in an approved sterilization package and stored after sterilization in accordance with the rules in force for sterile products. It is important that only such methods of sterilization and
  10. Steam sterilization
    Steam sterilization is carried out using saturated steam, usually at a temperature of 134 ° C. Staining as a result of the “shedding” of chemical indicators A large number of chemical indicators in one lot to be sterilized can lead to the formation of stains on the instruments, especially through direct contact. This concerns, first of all, silverware or with a silver-plated surface.
  11. Low temperature sterilization
    Low-temperature sterilization methods include gas and plasma sterilization. All these methods use chemicals with temperatures between 37 and 75 ° C. When choosing a low-temperature sterilization method, special attention should be paid to the treatment guidelines of the manufacturer of medical devices. Depending on the type, method and year of production of the sterilizers used
  12. Sterilization
    Sterilization is a fairly common method of contraception in families where women are over 40. This is an irreversible process that one spouse undergoes. In women, the fallopian tubes are ligated, in men, the vas deferens is excised. • Dressing, cauterization In women, sterilization is carried out by dressing, and dividing into parts of a specific area of ​​both uterine
  13. Section 57. Medical Sterilization
    1. Medical sterilization as a special medical intervention in order to deprive a person of the ability to reproduce offspring or as a method of contraception can be carried out only by a written statement of a citizen over the age of thirty-five or a citizen who has at least two children, and if there are medical indications and informed voluntary consent of a citizen -
  14. Hot air sterilization
    Although hot air sterilization no longer corresponds to the current level of science, in some cases this method is still used. If hot air sterilization is applied, the following requirements must be met: At temperatures from 185 ° C, paraffin oil is tarred, as a result of which its lubricity is lost and the performance of the instrument is reduced. Do not exceed
  15. Voluntary surgical sterilization
    Voluntary surgical sterilization (DHS) is given a special place in the family planning program, since, firstly, this method is associated with surgical intervention and, secondly, it is irreversible. Currently, DHS is the most common method of birth control in both developed and developing countries (according to world statistics, in 1990, DHS
  16. The staff of the Scientific Research Institute of Atmospheric Air Protection (Institute of Atmosphere). Methodological manual on the calculation, regulation and control of emissions of pollutants into the air, 2005
    The manual contains methodological recommendations, explanations and additions on the main issues of air protection activities: - inventory of emissions of harmful (polluting) substances into the atmospheric air and their sources; - rationing of emissions and the establishment of standards for PDV (VSV); - monitoring compliance with established emission standards; - summary calculations of air pollution emissions
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