11.120.20 – Wound dressings and compresses – PDF Standards Store ?u= Tue, 05 Nov 2024 15:40:26 +0000 en-US hourly 1 https://wordpress.org/?v=6.7.1 ?u=/wp-content/uploads/2024/11/cropped-icon-150x150.png 11.120.20 – Wound dressings and compresses – PDF Standards Store ?u= 32 32 DIN EN 13726:2021 Edition ?u=/product/publishers/din/din-en-13726/ Tue, 05 Nov 2024 15:40:26 +0000 Test methods for wound dressings - Aspects of absorbency and moisture vapour transmission, waterproofness and conformability (Draft)
Published By Publication Date Number of Pages
DIN 2021-02 122
]]>
This document specifies test methods for the evaluation of different performance characteristics of wound dressings, including absorbency, moisture vapour transmission rate, waterproofness and conformability.

]]>
DIN 61632:2009 Edition ?u=/product/publishers/din/din-61632/ Tue, 05 Nov 2024 15:16:25 +0000 Verbandmittel - Idealbinden
Published By Publication Date Number of Pages
DIN 2009-12 7
]]>
Diese Norm beschreibt IdeaIbinden als Verbabdmittel. Die Norm legt Gewebekonstruktion, Abmessung, Werkstoff und Ausführung fest. Weiterhin enthält sie Angaben über Prüfung und Kennzeichnung der Binden.*Inhaltsverzeichnis

]]>
DIN 13151:2008 Edition ?u=/product/publishers/din/din-13151/ Tue, 05 Nov 2024 15:10:20 +0000 Verbandmittel - Verbandpäckchen
Published By Publication Date Number of Pages
DIN 2008-12 4
]]>
Die Norm gilt für sterile Verbandpäckchen, die im Erste-Hilfe-Bereich verwendet werden.*Inhaltsverzeichnis

]]>
AS/NZS 2869:1998 ?u=/product/publishers/as/as-nzs-28691998/ Tue, 05 Nov 2024 13:28:15 +0000 Tampons - Menstrual
Published By Publication Date Number of Pages
AS 1998-05-05 37
]]>
Specifies requirements for menstrual tampons including length, pull strength and water repellency of the withdrawal cord, materials, absorptive capacity, microbial content, marking and packaging. Includes a classification system based on tampon absorbency with descriptive terms to be used in labelling tampons according to their absorbency range. Information to be given in an accompanying leaflet is described.

]]>
AS 2869:2022 ?u=/product/publishers/as/as-28692022/ Tue, 05 Nov 2024 12:45:42 +0000 Tampons - Menstrual
Published By Publication Date Number of Pages
AS 2022-05-06 44
]]>
AS 2869:2022 specifies requirements for menstrual tampons, including the specific absorptive capacity, microbial content, withdrawal cord pull strength and water repellency, marking and packaging. It also provides sample information to be included in an accompanying leaflet, such as information about toxic shock syndrome, precautions and instructions for correct use.

]]>
AS 2869:2008 ?u=/product/publishers/as/as-28692008/ Tue, 05 Nov 2024 12:45:41 +0000 Tampons - Menstrual
Published By Publication Date Number of Pages
AS 2008-08-08 37
]]>
Specifies requirements for menstrual tampons, including the specific absorptive capacity, microbial content, withdrawal cord pull strength and water repellency, marking and packaging. Information to be included in an accompanying leaflet is described.

Scope

This Standard specifies requirements for menstrual tampons, including the specific absorptive capacity, microbial content, withdrawal cord pull strength and water repellency, marking and packaging. Information to be included in an accompanying leaflet is described.

]]>
AS 2835.2:1998 ?u=/product/publishers/as/as-2835-21998/ Tue, 05 Nov 2024 12:45:19 +0000 Absorbent woven gauze - Cotton-viscose blends
Published By Publication Date Number of Pages
AS 1998-02-05 10
]]>
Specifies requirements for the cotton-viscose blends used in the manufacture of absorbent woven cotton gauze.

Scope

This Standard specifies requirements for absorbent woven gauze comprised of cotton and up to 53 percent viscose, suitable for use in the manufacture of surgical dressings.

]]>
AS 2835.1:1998 ?u=/product/publishers/as/as-2835-11998/ Tue, 05 Nov 2024 12:45:18 +0000 Absorbent woven gauze - Cotton
Published By Publication Date Number of Pages
AS 1998-02-05 9
]]>
Specifies requirements for absorbent woven cotton gauze suitable for use in the manufacture of surgical dressings.

]]>
BS EN 17854:2024 ?u=/product/publishers/bsi/bs-en-178542024/ Sun, 20 Oct 2024 09:51:59 +0000 Antimicrobial wound dressings. Requirements and test method
Published By Publication Date Number of Pages
BSI 2024 50
]]>
PDF Catalog
PDF Pages PDF Title
2 undefined
8 1 Scope
2 Normative references
3 Terms, definitions, symbols and abbreviated terms
3.1 Terms and definitions
10 3.2 Symbols and abbreviated terms
11 4 Requirements
4.1 Documentation and training
12 4.2 Microbicidal dressings
4.3 Microbistatic dressings
4.4 Performance table
5 Test method
5.1 Principle
13 5.2 General conditions
5.2.1 Volumes
5.2.2 Agar plates
5.3 Materials and reagents
5.3.1 Test organism strains
5.3.1.1 Storage of organisms
5.3.1.2 Bacteria
5.3.1.3 Yeast
14 5.3.1.4 Additional test organism strains
5.3.2 Reagents and culture media
5.3.2.1 General
5.3.2.2 Water
5.3.2.3 Tryptone Soya Broth (TSB)
15 5.3.2.4 Tryptone Soya Agar (TSA)
5.3.2.5 Simulated Wound Fluid (SWF)
5.3.2.6 Maximum recovery diluent (MRD)
5.3.2.7 Sabouraud broth (SAB)
5.3.2.8 Sabouraud agar (SAA)
16 5.3.2.9 Neutralizer
5.3.3 Test apparatus
17 5.4 Preparation of test and negative control dressings
5.5 Calculation of saturation volume and working volume
19 5.6 Preparation of test organism suspensions
5.6.1 Bacteria
20 5.6.2 Yeast
5.6.3 Preparation of STOCK A
21 5.7 Neutralization validation
5.7.1 General
5.7.2 Preparation of inoculum
22 5.7.3 Neutralizer toxicity
5.7.4 Test organism viability
5.7.5 Neutralizer efficacy
23 5.7.6 Interpretation of data
25 5.8 Procedure
5.8.1 Exposing the test and negative control dressings to test organisms
27 5.8.2 Recovery and enumeration of test organisms
28 5.8.3 Calculation and expression of results
30 5.8.4 Calculation of the detection limit of the test
31 5.8.5 Judgement of test validity
5.9 Test report
33 Annex A (informative)Referenced test organism strains in other national collections
34 Annex B (informative)Validation of neutralization
B.1 Principle
B.2 Neutralizer selection
35 Annex C (informative)Neutralizers
36 Annex D (informative)Rationale
D.1 General
D.2 Title
D.3 Test organism strains
37 D.4 Preparation of test organism suspensions
D.5 Cutting dressings
D.6 Positive control
D.7 Performance requirements
38 D.8 Media
D.9 Incubation temperatures
D.10 Dressing classification
D.11 Saturation volume
D.12 Procedure
39 D.13 Exposure times
D.14 Pre-conditioning and repeat challenge testing
D.15 Humidity
D.16 Recovery of test organisms from dressings
40 Annex E (informative)Replicates
41 Annex F (informative)Test method illustrations
46 Annex G (informative)Example Test Report Tables
]]>
ASTM-F1862/F1862M:2024 Edition(Redline) ?u=/product/publishers/astm/astm-f1862-f1862m-6/ Sun, 20 Oct 2024 09:40:46 +0000 F1862/F1862M-24 Standard Test Method for Resistance of Medical Face Masks to Penetration by Synthetic Blood (Horizontal Projection of Fixed Volume at a Known Velocity) (Redline)
Published By Publication Date Number of Pages
ASTM 2024 28
]]>
ASTM F1862/F1862M-24

Redline Standard: Standard Test Method for Resistance of Medical Face Masks to Penetration by Synthetic Blood (Horizontal Projection of Fixed Volume at a Known Velocity)

ASTM F1862/F1862M

Scope

1.1 This test method is used to evaluate the resistance of medical face masks to penetration by the impact of a small volume (~2 mL) of a high-velocity stream of synthetic blood. Medical face mask pass/fail determinations are based on visual detection of synthetic blood penetration.

1.2 This test method does not apply to all forms or conditions of blood-borne pathogen exposure. Users of the test method must review modes for face exposure and assess the appropriateness of this test method for their specific application.

1.3 This test method is primarily intended to address the performance of finished medical face masks. While this test method may also be used to assess performance of materials or certain material constructions used in medical face masks, it is important to note the performance of finished medical face masks may be impacted by the interaction of the materials used and how they have been assembled. Results can differ depending on testing a final finished medical face mask or materials taken from manufactured medical face masks.

1.4 This test method does not address other factors with the potential to affect the overall protection offered by the medical face mask and its operation (such as filtration efficiency and pressure drop).

1.5 This test method does not address breathability of the medical face mask materials or any other properties affecting the ease of breathing through the medical face mask. This test method evaluates medical face masks as an item of protective clothing. This test method does not evaluate the performance of medical face masks for airborne exposure pathways or in the prevention of the penetration of aerosolized body fluids deposited on the medical face mask.

1.6 The values stated in SI units or inch-pound units are to be regarded separately as standard. The values stated in each system may not be exact equivalents; therefore, each system shall be used independently of the other. Combining values from the two systems may result in nonconformance with the standard. The pressure values stated in each system are not exact equivalents. However, as the corresponding velocities are within 1 % of each other (see X1.4.2), reporting of the results in either units is permitted.

1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.

1.8 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

Keywords

blood; blood-borne pathogens; body fluids; medical face masks; penetration; synthetic blood;

ICS Code

ICS Number Code 11.120.20 (Wound dressings. Compresses)

DOI: 10.1520/F1862_F1862M-24

]]>