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BS EN ISO 10079-4:2021 Medical suction equipment General requirements

BS EN ISO 10079-4:2021

Medical suction equipment General requirements

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Standard number:BS EN ISO 10079-4:2021
Pages:44
Released:2021-10-20
ISBN:978 0 539 05142 1
Status:Standard
BS EN ISO 10079-4:2021 Medical Suction Equipment General Requirements

BS EN ISO 10079-4:2021 Medical Suction Equipment General Requirements

Ensure the highest standards of safety and performance with the BS EN ISO 10079-4:2021 Medical Suction Equipment General Requirements. This comprehensive standard is essential for manufacturers, healthcare providers, and regulatory bodies involved in the design, production, and use of medical suction equipment.

Overview

The BS EN ISO 10079-4:2021 standard provides detailed guidelines and requirements for medical suction equipment, ensuring that these critical devices meet stringent safety and performance criteria. Released on October 20, 2021, this standard is the latest in a series of updates aimed at maintaining the highest levels of patient care and equipment reliability.

Key Features

  • Standard Number: BS EN ISO 10079-4:2021
  • Pages: 44
  • Release Date: 2021-10-20
  • ISBN: 978 0 539 05142 1
  • Name: Medical Suction Equipment General Requirements
  • Status: Standard

Why Choose BS EN ISO 10079-4:2021?

Medical suction equipment is a vital component in various medical procedures, from routine surgeries to emergency interventions. The BS EN ISO 10079-4:2021 standard ensures that these devices are designed and manufactured to the highest quality, providing reliable performance when it matters most.

Comprehensive Guidelines

This standard covers a wide range of requirements, including:

  • Design and construction
  • Performance criteria
  • Safety features
  • Testing and validation procedures
  • Labeling and documentation

Enhanced Safety

Patient safety is paramount in any medical setting. The BS EN ISO 10079-4:2021 standard includes rigorous safety requirements to minimize risks associated with the use of medical suction equipment. This ensures that healthcare providers can trust the equipment to perform reliably and safely.

Global Recognition

As an internationally recognized standard, BS EN ISO 10079-4:2021 facilitates global trade and compliance. Manufacturers adhering to this standard can confidently market their products worldwide, knowing they meet the stringent requirements set by leading health authorities.

Who Should Use This Standard?

The BS EN ISO 10079-4:2021 standard is indispensable for a variety of stakeholders, including:

  • Medical device manufacturers
  • Healthcare providers
  • Regulatory bodies
  • Quality assurance professionals
  • Biomedical engineers

Detailed Content

With 44 pages of in-depth information, the BS EN ISO 10079-4:2021 standard provides a thorough understanding of the requirements for medical suction equipment. Each section is meticulously crafted to ensure clarity and comprehensiveness, making it an invaluable resource for anyone involved in the medical device industry.

Stay Ahead with the Latest Standards

Keeping up with the latest standards is crucial in the fast-evolving field of medical technology. The BS EN ISO 10079-4:2021 standard represents the cutting edge of medical suction equipment requirements, reflecting the latest advancements and best practices in the industry.

Conclusion

Investing in the BS EN ISO 10079-4:2021 Medical Suction Equipment General Requirements standard is a strategic decision that underscores your commitment to quality, safety, and excellence. Whether you are a manufacturer aiming to meet regulatory requirements or a healthcare provider seeking the best equipment for patient care, this standard is an essential tool in your arsenal.

Ensure your medical suction equipment meets the highest standards of performance and safety with the BS EN ISO 10079-4:2021 standard. Stay compliant, stay safe, and stay ahead in the ever-evolving world of medical technology.

DESCRIPTION

BS EN ISO 10079-4:2021


This standard BS EN ISO 10079-4:2021 Medical suction equipment is classified in these ICS categories:
  • 11.040.10 Anaesthetic, respiratory and reanimation equipment

This document specifies general requirements for medical suction equipment that are common to all parts of the ISO 10079 series .

This document is not applicable to the following:

  1. end-pieces such as suction catheters, drains, curettes, Yankauer suckers and suction tips;

  2. syringes;

  3. dental suction equipment;

  4. anaesthetic gas scavenging systems;

  5. laboratory suction;

  6. autotransfusion systems;

  7. mucus extractors including neonatal mucus extractors;

  8. suction equipment where the collection container is downstream of the vacuum pump;

  9. ventouse (obstetric) equipment;

  10. suction equipment marked for endoscopic use only; and

  11. plume evacuation systems.