BS EN ISO 8836:2020
Suction catheters for use in the respiratory tract
Standard number: | BS EN ISO 8836:2020 |
Pages: | 32 |
Released: | 2020-10-14 |
ISBN: | 978 0 580 98316 0 |
Status: | Standard |
BS EN ISO 8836:2020 Suction Catheters for Use in the Respiratory Tract
Introducing the BS EN ISO 8836:2020, a comprehensive standard that sets the benchmark for suction catheters used in the respiratory tract. This essential document is a must-have for healthcare professionals, medical device manufacturers, and regulatory bodies who are committed to ensuring the highest standards of patient care and safety.
Overview
The BS EN ISO 8836:2020 standard provides detailed guidelines and specifications for the design, performance, and testing of suction catheters. These catheters are critical tools in medical settings, used to clear the airways of patients who are unable to do so themselves. This standard ensures that the catheters meet stringent safety and efficacy requirements, thereby safeguarding patient health.
Key Features
- Standard Number: BS EN ISO 8836:2020
- Pages: 32
- Released: 2020-10-14
- ISBN: 978 0 580 98316 0
- Name: Suction catheters for use in the respiratory tract
- Status: Standard
Why Choose BS EN ISO 8836:2020?
This standard is indispensable for several reasons:
- Comprehensive Guidelines: It provides a thorough framework for the design and testing of suction catheters, ensuring they are safe and effective for patient use.
- International Recognition: As an ISO standard, it is recognized globally, facilitating international trade and compliance.
- Patient Safety: By adhering to this standard, healthcare providers can significantly reduce the risk of complications associated with the use of suction catheters.
- Quality Assurance: Manufacturers can use this standard to ensure their products meet the highest quality benchmarks, enhancing their reputation and reliability in the market.
Applications
The BS EN ISO 8836:2020 standard is applicable in various settings, including:
- Hospitals and Clinics: Ensuring that suction catheters used in these environments are up to standard, thereby improving patient outcomes.
- Medical Device Manufacturing: Providing manufacturers with the necessary guidelines to produce high-quality suction catheters that meet international standards.
- Regulatory Compliance: Assisting regulatory bodies in evaluating the safety and efficacy of suction catheters, ensuring they meet the required standards before being approved for use.
Detailed Content
The standard spans 32 pages, offering a detailed exploration of the following topics:
- Design Specifications: Detailed requirements for the physical and mechanical properties of suction catheters.
- Performance Criteria: Guidelines for testing the functionality and reliability of the catheters under various conditions.
- Safety Standards: Protocols to ensure the catheters do not pose any risk to patients or healthcare providers.
- Quality Control: Procedures for maintaining consistent quality in the production of suction catheters.
Conclusion
The BS EN ISO 8836:2020 standard is an invaluable resource for anyone involved in the design, manufacture, or use of suction catheters. By adhering to this standard, you can ensure that your products are safe, effective, and compliant with international regulations. This not only enhances patient safety but also boosts the credibility and marketability of your products.
Invest in the BS EN ISO 8836:2020 standard today and take a significant step towards excellence in healthcare and medical device manufacturing.
BS EN ISO 8836:2020
This standard BS EN ISO 8836:2020 Suction catheters for use in the respiratory tract is classified in these ICS categories:
- 11.040.10 Anaesthetic, respiratory and reanimation equipment
- 11.040.25 Syringes, needles and catheters
This document specifies dimensions and requirements for both open and closed suction catheters made of flexible materials and intended for use in suctioning of the respiratory tract.
Suction catheters intended for use with flammable anaesthetic gases or agents, lasers or electrosurgical equipment are not covered by this document.
For guidance on airway management during laser surgery of the upper airway, see ISO/TR 11991 [ 4 ].