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Skillfully Use Balm To Remove 3M Indication Tape Traces On Sterile Needle Box

  The most commonly used treatment tool in stomatology is car needle. After the patient's treatment, the car needle is placed in the aluminum car needle box for high-temperature pressure steam disinfection. When the 3M   sterilization indicaton tape  is pasted on the car needle box, so as to observe the disinfection effect. Long term repeated high-temperature and pressure steam disinfection makes it difficult to clean the traces of 3M sterilization indication tape left on the needle box. It is found that the traces left by 3M  sterilization indicator  tape can be easily wiped off with a dry cotton towel (no cleaning ball) after dropping the essence of wind oil on the traces of 3M  sterilization indicator  tape that are difficult to clean and remove for 30min to 1H. The 3M indicating tape trace on the needle box is removed by using air balm, which has a good effect and is worthy of popularization.
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If You Think Your Pouch is Just a Pouch, Wait Until You Read This

  Do you know what self sealing sterilization pouches are? If not, then read on to learn more about these amazing products. A self-sealing sterilization pouch is a bag that can be sealed and opened with one hand and contains an atmosphere that will destroy bacteria and other microorganisms in the bag's contents.   Self seal sterilization pouches   have been used for decades in hospitals worldwide because they offer excellent protection against contamination of medical instruments, surgical equipment, or pharmaceuticals during transport or storage. When self sealing sterilization pouches are used to package medical devices or pharmaceuticals, the self seal sterilization pouch provides a barrier that protects these products against moisture and contamination during shipping. This helps ensure that when your customers use them in their procedures, they will be safe for patient care. What do you truly understand about the sterilization pouches you use? What should you be aware of? What

Definition And Use Of Sterilization Or Chemical Indicator

  Sterilization indicator  tape and label   Definition: Wrinkle paper or label paper as the base material, coated with color-changing ink as sterilization indicator, back coated with pressure sensitive adhesive.  The indicating tape used for chemical monitoring outside the pressure steam  sterilization package , when reaching certain sterilization conditions 121℃, 20 minutes or 132℃, 3 minutes, the chemical indicating stripe on the back base of wrinkled paper will change from light yellow to black.   USES:   1. Used to mark whether the package has been treated by pressure steam sterilization process.   2. If the discoloration is uneven or incomplete, it may indicate that the package has not been sterilized in accordance with the conditions.   3, wrap the parcel (if no sealing tape is used).   4, sterilization information can be recorded (operator, sterilization period, item name, pot, etc.).   Chemical instruction card for plasma sterilization   Definition: rectangular paper structure,

Correctly Identify Discoloration of Chemical Indicator Cards

  01   Sterilization pouches   requirements   Why packaging   After a proper sterilization process, the apparatus in the sterilization room should be sterile, but when the apparatus is removed from the sterilization room, the outdoor air contains dust particles and microorganisms   If the device is not packaged, it will soon be contaminated   In addition, sterile items usually need to be stored for a period of time and sent to the department in need, so the equipment must be properly packaged to prevent re-contamination   Sterilization packaging  management requirements   Packaging purpose:   Extend the effect of sterilization to ensure that sterile equipment and articles can remain sterile before use.   Strict packaging requirements:   Surgical instruments use closed packaging method, generally 2 layers of packaging materials.  Closed type packaging application of special tape, tight sealing package.   The weight of the instrument bag shall not exceed 7 kg, and the weight of the dress

Medical Sealing Machine Operation & Maintenance Manual(II)

  XI. Operation Qualification (0Q) According to 5.7.10 Sealing and Packaging Requirements,Part II: Standard for Operating Procedures of Cleaning,Disinfection and Sterilization,WS310.2-2016 Central Sterile Supply Department (CSSD) and relevant regulations in GB/T19633.2-2015/ISO11607-2:2006, the accuracy of parameters and the sealing quality of the machine should be inspected before it works every day. Therefore,test cards and sealing strength testers should be used for OQ. OQ refers to the sealing performance verification during the normal operation of the  machine. To test whether the sealing edge has any tube-like space or opening; To test whether the pressure is too high or too low; To test whether the sealing temperature is too high or too low; To test whether sealing is continuous or the sealing edge has leaks; It is suggested that users should finish the sealing test before and after daily sealing work,and the test sample should be stored for query. To inspect and record operatio

Medical Sealing Machine Operation & Maintenance Manual(I)

  I. About Thank you for choosing  KM100 series of sealing machine . To maximize its performance,please carefully read this manual and install and operate it by strictly following this manual to ensure its safety and reliability in use. We recommend placing the manual in an accessible place for better reference during the operation. II. Applied Area Automatic  medical sealing machine , 100-L series, is capable of continuous paper-plastic bag, 3D paper-plastic bag and paper-paper bag sealing. The sealing process satisfies the requirements of high-temperature steam sterilization, low-temperature ethylene oxide sterilization, hydrogen peroxide plasma sterilization and radiation sterilization. Seal quality meets corresponding international standards and GMP recognition. Sealable materials: Compliance with EN868-5 and YY/T 0698-5 bags and volumes; Compliance with EN868-4 and YY/T0698-4 paper bags; High density polyethylene materials (such as Tyvek); Aluminum foiled materials. Non-sealable m