PD CEN/TR 16953:2017

European foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Considerations in glove selection
5 Raw materials
6 Glove disinfection
7 Labelling
Annex A (informative) - Glove materials and their use
Annex B (informative) - Additional information
Annex C (informative) - CE-Marking
Bibliography

Defines information for those choosing or using sterile and non-sterile gloves for medical applications based on a risk assessment.

This Technical Report provides information for those choosing or using sterile and non-sterile gloves for medical applications based on a risk assessment. It deals with gloves worn primarily for the protection of the patient and glove user from biological cross contamination. NOTE Gloves worn specifically for the protection of the glove user from e.g. chemical and biological hazards are covered by the EU-Directive on Personal Protective Equipment (PPE) and the related standards e.g. EN 16523-1, EN 374-2, EN 374-4, EN ISO 374-1 and EN ISO 374-5. This document describes the rationale behind the requirements of the EN 455 series and explores the possible trade-offs in glove selection between the various factors which affect glove, physical properties, biocompatibility, comfort and sensitivity. The strengths and weaknesses of various alternative glove materials and the potential biological hazards presented by their use are also explored.