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ISO 11737-1:2006, Sterilization of medical devices - Microbiological methods - Part 1: Determination of a population of microorganisms on products Paperback August 23, 2007
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ISO 11737-1:2006, Sterilization of medical devices - Microbiological methods - Part 1: Determination of a population of microorganisms on products Paperback August 23, 2007
ISO 11737-1:2006 specifies requirements and provides guidance for the enumeration and microbial characterization of the population of viable microorganisms on or in a medical device, component, raw material or package.
ISO 11737-1:2006, Sterilization of medical devices - Microbiological methods - Part 1: Determination of a population of microorganisms on products Paperback August 23, 2007
Item #: 19636416

ISO 11737-1:2006, Sterilization of medical devices - Microbiological methods - Part 1: Determination of a population of microorganisms on products

Item #: 19636416

SCR 1911

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ISO 11737-1:2006 specifies requirements and provides guidance for the enumeration and microbial characterization of the population of viable microorganisms on or in a medical device, component, raw material or package.
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What Stands Out

Standard Compliance
Adheres to ISO 11737-1:2006 standards, ensuring reliable methodologies for determining microorganism populations on medical devices, enhancing safety and efficacy in healthcare settings.
Comprehensive Guide
Offers detailed insights into microbiological testing methods, serving as an essential reference for quality assurance professionals in the medical device industry.
Expert Validation
Published by reputable sources, providing authoritative information backed by industry experts, ensuring users have trustworthy guidance for sterilization protocols.

Product Details

Shop ISO 11737-1:2006, Sterilization of medical devices - Microbiological methods - Part 1: Determination of a population of microorganisms on products Paperback August 23, 2007 online at a best price in Seychelles. B000Y2U7SO
  • Specifies requirements and guidance for enumerating and characterizing the population of viable microorganisms on or in medical devices, components, raw materials, or packages
  • Does not cover enumeration or identification of viral or protozoan contaminants
  • Does not cover microbiological monitoring of the environment in which medical devices are manufactured
  • Part of the ISO 11737 standard for sterilization of medical devices
  • Provides essential methods for determining microbial population on products
  • Published in paperback on August 23, 2007
Item Weight1 lbs (450 grams)

Who Should Buy?

Suitable For
  • Medical Device Manufacturers

    Essential for manufacturers needing reliable methods to determine microbial population for sterilization validation processes.

  • Quality Control Personnel

    Quality control teams can effectively ensure compliance with sterilization standards using this comprehensive microbiological method.

  • Regulatory Compliance Officers

    Helps officers understand and implement necessary protocols to meet regulatory requirements for medical device sterilization.

Not Suitable For
  • General Consumers

    Not suitable for everyday consumers as it addresses technical sterilization processes outside their scope of understanding.

  • Small Clinics

    Small clinics may lack the resources and need for detailed microbiological methods outlined in the product.

  • Non-medical Industries

    Not relevant for users in non-medical fields, as the methods are specifically tailored for medical device applications.

Product Description

ISO 11737-1:2006, Sterilization of medical devices - Microbiological methods - Part 1: Determination of a population of microorganisms on products Paperback August 23, 2007

About This Item

Introducing the ISO 11737-1:2006 Paperback, a comprehensive guide for sterilization of medical devices using microbiological methods. When it comes to medical devices, ensuring proper sterilization is of utmost importance. The ISO 11737-1:2006 standard is designed to help manufacturers and healthcare professionals determine the population of microorganisms on products, guaranteeing that they meet the necessary safety and quality requirements. This book is an invaluable resource for anyone involved in the sterilization of medical devices. It provides detailed information on the ISO 11737-1:2006 standard, covering topics such as testing methods, regulations, and validation processes.

By following these guidelines, you can ensure your medical devices are properly sterilized, protecting patients and minimizing the risk of infection. With this paperback, you will gain a comprehensive understanding of the ISO 11737-1:2006 standard and its implications for medical devices. Whether you are a manufacturer looking to comply with the regulations or a healthcare professional responsible for validating sterilization processes, this book is a must-have reference. Stay ahead of the curve and guarantee the safety of your medical devices by investing in the ISO 11737-1:2006 Paperback today. Order now and take the necessary steps to meet the highest sterilization standards in the industry.

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Customer Questions & Answers

  • Question: What is ISO 11737-1:2006?

    Answer: ISO 11737-1:2006 is a standard that outlines microbiological methods for sterilization of medical devices, specifically focusing on the determination of microorganism populations on products. This standard ensures that medical devices meet safety and efficacy requirements by providing a protocol for quantifying microbial loads. It is crucial for manufacturers to adhere to this standard to minimize risks associated with medical devices, thereby protecting patient health and ensuring compliance with regulatory requirements.
  • Question: Why is the determination of microorganisms important in medical devices?

    Answer: Determining microorganism populations is critical in ensuring the safety and sterility of medical devices. By quantifying microbial presence, manufacturers can implement effective sterilization processes and ensure compliance with health regulations. This process is essential in preventing infections during medical procedures. For instance, devices used in surgery must have a validated sterility assurance to protect patients from potential complications caused by microbial contamination.
  • Question: How is the population of microorganisms determined as per ISO 11737-1:2006?

    Answer: The population of microorganisms is determined through a series of laboratory tests that quantify viable organisms on the device surfaces. This typically involves sampling, culturing, and enumerating the microorganisms present. Understanding microbial load helps manufacturers establish effective sterilization protocols that align with industry standards. For example, a device that undergoes rigorous microbial assessment can be confidently used in sterile environments, ensuring its safety for patient use.
  • Question: Who needs to follow ISO 11737-1:2006 standards?

    Answer: ISO 11737-1:2006 standards are essential for manufacturers of medical devices looking to market their products in regulated environments. This includes entities involved in the design, production, and testing of surgical instruments, implants, and other related devices. Compliance with these standards is vital not only for accessing the market but also for preserving patient trust in healthcare products. For example, hospitals rely on such standards to ensure that the tools used in surgeries are safe from microbial contamination.
  • Question: What types of medical devices does ISO 11737-1:2006 apply to?

    Answer: ISO 11737-1:2006 applies broadly to a variety of medical devices that require sterilization prior to use. This includes surgical instruments, implants, diagnostic tools, and other products that come into contact with sterile environments or tissues. Compliance ensures that these devices do not introduce harmful microorganisms into the body, which can lead to serious health concerns. For instance, an implantable device must meet these standards to ensure it is safe for long-term usage by patients.
  • Question: How often should testing be done as per ISO 11737-1:2006?

    Answer: The frequency of testing according to ISO 11737-1:2006 often depends on the specific manufacturing process and regulatory guidelines. However, it is generally recommended to conduct microbial assessments at key phases of production, such as after cleaning, pre-sterilization, and before final packaging. This ongoing assessment helps to maintain product integrity and safety across batches of medical devices. For example, continuous monitoring during production could identify potential contamination risks before the devices reach the market.
  • Question: What are the consequences of not following ISO 11737-1:2006?

    Answer: Failing to adhere to ISO 11737-1:2006 can lead to severe consequences, including product recalls, regulatory fines, and loss of market access. Moreover, non-compliance can endanger patient safety due to the risk of infection from contaminated devices. This can result in legal liability and damage to a company’s reputation. For example, a medical device company that overlooks these standards may face lawsuits if their products lead to infections during medical procedures.
  • Question: Can ISO 11737-1:2006 be implemented in all countries?

    Answer: ISO 11737-1:2006 can theoretically be implemented in any country; however, its adoption may vary based on national regulations and standards for medical device manufacturing. Countries with stringent healthcare regulatory environments are more likely to mandate compliance with ISO standards. For instance, in countries with established regulations, manufacturers must align their processes with ISO 11737-1:2006 to ensure product approval for market entry.
  • Question: How does ISO 11737-1:2006 improve patient safety?

    Answer: ISO 11737-1:2006 enhances patient safety by providing a reliable framework for assessing the sterility of medical devices. By ensuring that devices are free from harmful microorganisms, this standard helps prevent infection and enhances the efficacy of treatments. For example, surgical instruments adhering to this standard contribute to safer surgical outcomes, thereby improving overall patient care and trust in medical practices.
  • Question: Where can I buy ISO 11737-1:2006 in Seychelles?

    Answer: You can purchase ISO 11737-1:2006 through Ubuy in Seychelles. Ubuy is a reliable online platform that offers a variety of standards and publications, ensuring you have access to the necessary resources for compliance and quality assurance in medical device manufacturing. Their user-friendly interface makes it easy to find and order the specific standard you need.

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SCR 1911

Order now and get it around Friday, July 03

QTY:

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Ubuy works hard to protect your security and privacy. Our advanced payment security system ensures confidentiality by encrypting your information during transmission using AES (Advanced Encryption Standards) and SSL (Secure Socket Layer) protocols. Your payment details are 100% secure as we do not share your payment details with third party sellers.

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Features & Benefits

  • ISO 11737-1:2006 provides guidance for the enumeration and microbial characterization of microorganisms on medical devices
  • Does not specify requirements for viral or protozoan contaminants
  • Does not specify requirements for microbiological monitoring of manufacturing environment