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Homepage>BSI Standards >11 HEALTH CARE TECHNOLOGY>11.140 Hospital equipment>BS EN 455-5:2025 Medical gloves for single use Extractable chemical residues
immediate downloadReleased: 2025-08-27

BS EN 455-5:2025

Medical gloves for single use Extractable chemical residues

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Standard number:BS EN 455-5:2025
Pages:26
Released:2025-08-27
ISBN:978 0 539 23967 6
Status:Standard
BS EN 455-5:2025 Medical Gloves for Single Use - Extractable Chemical Residues

BS EN 455-5:2025 Medical Gloves for Single Use - Extractable Chemical Residues

Introducing the BS EN 455-5:2025, a comprehensive standard that sets the benchmark for medical gloves designed for single use, focusing on extractable chemical residues. This standard is an essential resource for manufacturers, healthcare professionals, and regulatory bodies who are committed to ensuring the highest level of safety and quality in medical gloves.

Key Features of BS EN 455-5:2025

  • Standard Number: BS EN 455-5:2025
  • Pages: 26
  • Release Date: August 27, 2025
  • ISBN: 978 0 539 23967 6
  • Status: Standard

Why Choose BS EN 455-5:2025?

The BS EN 455-5:2025 standard is meticulously crafted to address the critical aspect of extractable chemical residues in medical gloves. These residues can pose potential risks to both healthcare providers and patients, making it imperative to adhere to stringent guidelines. This standard provides a detailed framework for testing and evaluating the chemical residues that may be present in medical gloves, ensuring they meet the necessary safety requirements.

Comprehensive Coverage

With 26 pages of in-depth information, the BS EN 455-5:2025 standard offers a thorough examination of the procedures and criteria for assessing chemical residues. It covers a wide range of topics, including:

  • Methods for detecting and quantifying chemical residues
  • Acceptable limits for various chemical substances
  • Guidelines for manufacturers to minimize chemical residues during production
  • Recommendations for testing and quality control

Ensuring Safety and Compliance

Compliance with the BS EN 455-5:2025 standard is crucial for manufacturers aiming to produce medical gloves that are safe for use in healthcare settings. By adhering to this standard, manufacturers can demonstrate their commitment to quality and safety, thereby gaining the trust of healthcare professionals and regulatory authorities.

Benefits for Healthcare Professionals

For healthcare professionals, using gloves that comply with the BS EN 455-5:2025 standard means enhanced protection against potential chemical exposure. This standard helps ensure that the gloves used in medical procedures are free from harmful levels of chemical residues, thereby reducing the risk of adverse reactions and ensuring patient safety.

Who Should Use This Standard?

The BS EN 455-5:2025 standard is an invaluable resource for a wide range of stakeholders, including:

  • Medical glove manufacturers seeking to ensure product safety and compliance
  • Quality assurance professionals responsible for testing and certifying medical gloves
  • Regulatory bodies overseeing the safety standards of medical products
  • Healthcare institutions committed to providing safe and reliable medical supplies

Conclusion

The BS EN 455-5:2025 standard is a critical tool in the pursuit of safety and quality in the production and use of medical gloves. By providing clear guidelines and rigorous testing methods, this standard helps ensure that medical gloves are free from harmful chemical residues, thereby protecting both healthcare providers and patients. Whether you are a manufacturer, a healthcare professional, or a regulatory authority, the BS EN 455-5:2025 standard is an essential resource for maintaining the highest standards of safety and quality in medical gloves.

DESCRIPTION

BS EN 455-5:2025


This standard BS EN 455-5:2025 Medical gloves for single use is classified in these ICS categories:
  • 11.140 Hospital equipment
This document specifies a test method for the measurement of residual chemicals used in product manufacture, particularly potentially Type IV allergenic substances employed and remaining in medical gloves. It also provides information on the extraction medium, the method of extraction and quantitative assay of residual chemicals. This document does not provide information on the allergenic potential, biological evaluation, or safety to the user of any product.