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…
Evaluation of Single-Use Medical Sharps Containers for Biohazardous and Cytotoxic Waste
1 Scope
1.1
This Standard applies to the material of construction, the physical integrity, and the labelling requirements of biohazardous and cytotoxic medical sharps containers.
1.2
This Standard applies to medical sharps containers intended for single use.
1.3
This Standard specifies test criteria for the evaluation of the following characteristics of sharps containers:
a)…
Evaluation of Single Use Medical Sharps Containers for Biohazardous and Cytotoxic Waste
1. Scope
1.1
This Standard applies to the material of construction, the physical integrity, and the labelling requirements of biohazardous and cytotoxic medical sharps containers.
1.2
This Standard applies to medical sharps containers intended for single use.
1.3
This Standard states test criteria for the evaluation of the following characteristics of sharps containers:
(a)…
Fans — Determination of fan sound power levels under standardized laboratory conditions — Part 1: Ge...
This document establishes principles for the determination of the acoustic performance of fans. In addition, this document can be used to determine the acoustic performance of fans combined with an ancillary device such as a roof cowl or damper or, where the fan is fitted with a silencer, the sound power resulting from the fan and silencer combination.
Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-2...
IEC 61010-2-201:2024 EXV contains both the international standard and its extended version (EXV). This extended version of the official IEC Standard is available in English only and provides the user with a comprehensive content of the Standard. IEC 61010-2-201:2024 EXV includes the content of the references made to IEC 61010-1:2010+AMD1:2016 CSV.
IEC 61010-2-201:2024 supplements or modifies…
Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-2...
IEC 61010-2-201:2024 supplements or modifies the corresponding clauses in IEC 61010-1 so as to convert that publication into the IEC standard: Particular requirements for control equipment. This document is to be used in conjunction with IEC 61010-1:2010, and IEC 61010 1:2010/AMD1:2016. Where a particular subclause of IEC 61010-1 is not mentioned in this document, that subclause applies as far as…
Clinical laboratory testing and in vitro medical devices — Requirements for in vitro monitoring syst...
This document specifies requirements for in vitro measuring systems for self-monitoring of vitamin-K antagonist oral anticoagulation therapy, including performance, quality assurance and user training and procedures for the validation of performance by the intended users under actual and simulated conditions of use.
This document applies solely to prothrombin time measuring systems used by lay…
Safety requirements for electrical equipment for measurement, control, and laboratory use — Part 2-0...
1.1 Scope
[Add the following]
This Standard applies to the above-noted equipment that is intended to be installed or used in
accordance with CSA C22.1, Canadian Electrical Code, Part I.
General requirements applicable to this Standard are provided in CAN/CSA-C22.2 No. 0.
