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Homepage>BS Standards>11 HEALTH CARE TECHNOLOGY>11.040 Medical equipment>11.040.55 Diagnostic equipment>BS EN IEC 61010-2-101:2022+A11:2022 Safety requirements for electrical equipment for measurement, control, and laboratory use Safety requirements for in vitro diagnostic (IVD) medical equipment
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BS EN IEC 61010-2-101:2022+A11:2022 Safety requirements for electrical equipment for measurement, control, and laboratory use Safety requirements for in vitro diagnostic (IVD) medical equipment

BS EN IEC 61010-2-101:2022+A11:2022

Safety requirements for electrical equipment for measurement, control, and laboratory use Safety requirements for in vitro diagnostic (IVD) medical equipment

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Standard number:BS EN IEC 61010-2-101:2022+A11:2022
Pages:30
Released:2023-04-28
ISBN:978 0 539 18045 9
Status:Standard

BS EN IEC 61010-2-101:2022+A11:2022 Safety Requirements for Electrical Equipment for Measurement, Control, and Laboratory Use Safety Requirements for In Vitro Diagnostic (IVD) Medical Equipment

Introducing the BS EN IEC 61010-2-101:2022+A11:2022, a comprehensive guide to safety requirements for electrical equipment used in measurement, control, and laboratory settings, with a special focus on in vitro diagnostic (IVD) medical equipment. This standard is a must-have for professionals in the field, ensuring the highest level of safety and compliance in the workplace.

Key Features

The BS EN IEC 61010-2-101:2022+A11:2022 is a 30-page document, packed with essential information and guidelines. It is the latest release, published on April 28, 2023, ensuring the most up-to-date and relevant content for users. The standard carries the ISBN number 978 0 539 18045 9, making it easily identifiable and accessible in libraries and databases worldwide.

Why Choose BS EN IEC 61010-2-101:2022+A11:2022?

As a professional in the field of measurement, control, and laboratory use, safety should be your top priority. This standard provides a comprehensive set of safety requirements for electrical equipment, ensuring that you can carry out your work with confidence and peace of mind. The inclusion of safety requirements for in vitro diagnostic (IVD) medical equipment makes this standard particularly valuable for those working in medical and healthcare settings.

By adhering to the BS EN IEC 61010-2-101:2022+A11:2022, you can ensure that your equipment is safe, reliable, and compliant with international standards. This not only protects you and your colleagues but also enhances the credibility and reputation of your organization.

What's Inside?

The BS EN IEC 61010-2-101:2022+A11:2022 covers a wide range of topics, including but not limited to:

  • General safety requirements for electrical equipment
  • Specific safety requirements for equipment used in measurement, control, and laboratory use
  • Detailed safety requirements for in vitro diagnostic (IVD) medical equipment

Each section is clearly laid out and easy to understand, making it a valuable resource for professionals at all levels of experience.

Conclusion

The BS EN IEC 61010-2-101:2022+A11:2022 is more than just a standard; it's a commitment to safety, quality, and professionalism. Whether you're a seasoned professional or just starting out in the field, this standard is an invaluable tool for ensuring the highest level of safety in your work. Don't compromise on safety – choose the BS EN IEC 61010-2-101:2022+A11:2022 today.

Status: Standard

DESCRIPTION

BS EN IEC 61010-2-101:2022+A11:2022


This standard BS EN IEC 61010-2-101:2022+A11:2022 Safety requirements for electrical equipment for measurement, control, and laboratory use is classified in these ICS categories:
  • 11.040.55 Diagnostic equipment
  • 19.080 Electrical and electronic testing
  • 71.040.10 Chemical laboratories. Laboratory equipment