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BS EN ISO 22612:2005

Current

Current

The latest, up-to-date edition.

Clothing for protection against infectious agents. Test method for resistance to dry microbial penetration

Available format(s)

Hardcopy , PDF

Language(s)

English

Published date

23-03-2005

€156.59
Excluding VAT

Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Principle
5 Testing conditions
6 Equipment
  6.1 General lay-out
  6.2 Test containers
  6.3 Method to infect talc with spores
      6.3.1 Materials
      6.3.2 Procedure
7 Procedure
8 Test report
Annex A (informative) Preparation of TGE agar medium
  A.1 Ingredients
  A.2 Procedure
Annex ZA (informative) Relationship between this European
                       Standard and the Essential Requirements
                       of EU Directive 93/42/EEC concerning
                       medical devices
Annex ZB (informative) Relationship between this European
                       Standard and the Essential Requirements
                       of EU Directive 89/686/EEC concerning
                       personal protective equipment
Annex ZC (normative) Normative references to international
                     publications with their relevant European
                     publications
Bibliography

Provides a means for assessing the resistance to penetration through barrier materials of bacteria-carrying particles.

Committee
CH/205
DevelopmentNote
Supersedes 03/107275 DC. (04/2005)
DocumentType
Standard
Pages
18
PublisherName
British Standards Institution
Status
Current
Supersedes

This test method provides a means for assessing the resistance to penetration through barrier materials of bacteria-carrying particles.

NOTE Due to its complexity, this EN ISO22612 cannot be considered as a useful method for routine quality control but may suit the needs when a material is assessed for compliance with the requirements of current regulations such as EU Directive 93/42/EEC.

EN 13795-1:2002+A1:2009 Surgical drapes, gowns and clean air suits, used as medical devices, for patients, clinical staff and equipment - Part 1: General requirements for manufacturers, processors and products
89/686/EEC : 1989 AMD 5 2012 COUNCIL DIRECTIVE OF 21 DECEMBER 1989 ON THE APPROXIMATION OF THE LAWS OF THE MEMBER STATES RELATING TO PERSONAL PROTECTIVE EQUIPMENT
PREN 13795-3 : DRAFT 2004 SURGICAL DRAPES, GOWNS AND CLEAN AIR SUITS, USED AS MEDICAL DEVICES FOR PATIENTS, CLINICAL STAFF AND EQUIPMENT - PART 3: PERFORMANCE REQUIREMENTS

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