BS EN 455-3:2023 Medical Gloves for Single Use - Requirements and Testing for Biological Evaluation

Ensure the highest standards of safety and quality with the BS EN 455-3:2023 standard, specifically designed for medical gloves intended for single use. This comprehensive document outlines the essential requirements and testing methods for the biological evaluation of medical gloves, ensuring they meet stringent health and safety criteria.

Key Features and Benefits

The BS EN 455-3:2023 standard is an indispensable resource for manufacturers, healthcare providers, and regulatory bodies. Here are some of the key features and benefits:

• Comprehensive Guidelines: This standard provides detailed requirements and testing procedures to ensure the biological safety of medical gloves.
• Up-to-Date Information: Released on December 7, 2023, this document reflects the latest advancements and regulatory updates in the field.
• Enhanced Safety: By adhering to this standard, manufacturers can ensure their products are safe for use, reducing the risk of allergic reactions and other health issues.
• Quality Assurance: The standard helps in maintaining consistent quality across different batches of medical gloves, ensuring reliability and trustworthiness.
• Regulatory Compliance: Compliance with this standard is often a prerequisite for market approval in many regions, making it essential for manufacturers aiming for global reach.

Detailed Specifications

Here are the detailed specifications of the BS EN 455-3:2023 standard:

Standard Number	BS EN 455-3:2023
Pages	48
Released	2023-12-07
ISBN	978 0 539 15656 0
Name	Medical gloves for single use Requirements and testing for biological evaluation
Status	Standard

Why Choose BS EN 455-3:2023?

Choosing the BS EN 455-3:2023 standard means prioritizing safety, quality, and compliance. Here’s why this standard is a must-have:

1. Ensuring Patient Safety

Medical gloves are a critical component in preventing the transmission of infections. This standard ensures that the gloves are biologically safe, minimizing the risk of adverse reactions for both healthcare providers and patients.

2. Meeting Regulatory Requirements

Compliance with the BS EN 455-3:2023 standard is often required by regulatory bodies worldwide. Adhering to this standard can facilitate smoother market entry and approval processes.

3. Enhancing Product Quality

By following the guidelines and testing methods outlined in this standard, manufacturers can produce high-quality medical gloves that meet international safety and performance benchmarks.

4. Staying Current with Industry Standards

Released in December 2023, this standard incorporates the latest research and technological advancements, ensuring that your products are at the forefront of safety and innovation.

Who Should Use This Standard?

The BS EN 455-3:2023 standard is essential for a wide range of stakeholders in the healthcare and manufacturing sectors, including:

• Medical Glove Manufacturers: Ensure your products meet the highest safety and quality standards.
• Healthcare Providers: Use gloves that comply with this standard to protect both staff and patients.
• Regulatory Bodies: Reference this standard when evaluating the safety and efficacy of medical gloves.
• Quality Assurance Professionals: Implement the testing methods and requirements to maintain consistent product quality.

Conclusion

The BS EN 455-3:2023 standard is a vital document for anyone involved in the production, regulation, or use of medical gloves. By providing comprehensive guidelines and testing methods for biological evaluation, this standard ensures that medical gloves are safe, reliable, and of the highest quality.

Stay ahead in the industry by adopting the BS EN 455-3:2023 standard and ensure that your medical gloves meet the rigorous demands of modern healthcare.

BS EN 455-3:2023

This standard BS EN 455-3:2023 Medical gloves for single use is classified in these ICS categories:

• 11.140 Hospital equipment

This part of EN 455 specifies requirements for the evaluation of biological safety for medical gloves for single use. It gives requirements for labelling and the disclosure of information relevant to the test methods used.