Paints and varnishes — Determination of release rate of biocides from antifouling paints — Part 3: C...
ISO 15181-3:2007 specifies the apparatus and analytical method for determining the amount of zineb that has been released from an antifouling paint into artificial seawater in accordance with the procedure given in ISO 15181-1.
Zineb is released from antifouling paints in the form of ionic ethylene-bis(dithiocarbamate) which is unstable in the marine environment. This part of ISO 15181 describes…
Environmental testing - Part 3-11: Supporting documentation and guidance - Calculation of uncertaint...
Demonstrates how to estimate the uncertainty of steady-state temperature and humidity conditions in temperature and humidity chambers. Since this is inextricably linked to the methods of measurement, these are also described. This standard is equally applicable to all environmental enclosures, including rooms or laboratories. The methods used apply both to temperature chambers and combined…
Solar heating — Domestic water heating systems — Part 5: System performance characterization by mean...
ISO 9459-5:2007 specifies a method for outdoor laboratory testing of solar domestic hot-water (SDHW) systems. The method may also be applied for in-situ tests, and also for indoor tests by specifying appropriate draw-off profiles and irradiance profiles for indoor measurements. The system performance is characterized by means of whole-system tests using a 'black-box' approach, i.e. no…
Road vehicles — Cleanliness of components of fluid circuits — Part 5: Method of extraction of contam...
ISO 16232-5:2007 describes the principles of extraction of contaminants by test on a laboratory functional test bench with the test liquid flowing under pressure or under vacuum. It is applicable to both active and passive components through which the fluid can easily flow.
Unless otherwise specified, ISO 16232-5:2007 deals with particulate contamination only. It does not, therefore, cover…
Medical laboratories — Particular requirements for quality and competence
ISO 15189:2007 specifies requirements for quality and competence particular to medical laboratories.
ISO 15189:2007 is for use by medical laboratories in developing their quality management systems and assessing their own competence, and for use by accreditation bodies in confirming or recognising the competence of medical laboratories.
Clinical laboratory testing and in vitro medical devices — Requirements for in vitro monitoring syst...
ISO 17593:2007 specifies requirements for in vitro measuring systems for self-monitoring of vitamin-K antagonist therapy, including performance, quality assurance and user training and procedures for the verification and validation of performance by the intended users under actual and simulated conditions of use.
ISO 17593:2007 pertains solely to prothrombin time measuring systems used by…
Controlled equivalence ratio method for the determination of hazardous components of fire effluents
ISO/TS 19700:2007 describes a tube-furnace method for the generation of fire effluent for the identification and measurement of its constituent combustion products, in particular, the yields of toxic products under a range of fire decomposition conditions.
The test method described in ISO/TS 19700:2007 can be used solely to measure and describe the properties of materials, products or systems in…
ISO 212:2007 gives the general rules for the sampling of essential oils, in order to provide a laboratory with quantities that are suitable to be handled for expertise purposes.
Evaluation of Single-Use and Reusable Medical Sharps Containers for Biohazardous and Cytotoxic Waste
1 Scope
1.1
This Standard specifies test criteria for evaluating the following characteristics of single-use and reusable medical sharps containers for biohazardous and cytotoxic waste:
(a) materials of construction;
(b) colour;
(c) lifespan of reusable containers;
(d) puncture resistance;
(e) fill capacity and fill capacity indicator;
(f) overfill protection;
(g) needle unwinders;
(h) handle…
