Plastics — Methods of exposure to laboratory light sources — Part 3: Fluorescent UV lamps
ISO 4892-3:2016 specifies methods for exposing specimens to fluorescent UV radiation, heat and water in apparatus designed to simulate the weathering effects that occur when materials are exposed in actual end-use environments to global solar radiation, or to solar radiation through window glass.
The specimens are exposed to fluorescent UV lamps under controlled environmental conditions (…
ISO 669:2016 defines and specifies certain identified electrical and mechanical characteristics of equipment used for
- resistance spot welding,
- projection welding,
- resistance seam welding,
- upset welding[1], and
? flash welding[2].
ISO 669:2016 specifies the information to be given in equipment specifications and the test methods to be used for measuring those…
Anaesthetic vaporizers — Agent-specific filling systems
ISO 5360:2016 specifies requirements, including dimensions, for agent-specific filling systems for agent-specific anaesthetic vaporizers.
ISO 5360:2016 does not specify construction materials.
NOTE 1 For recommendations on materials, see Annex A.
Because of the unique properties of desflurane, dimensions for this agent have not been specified in this International Standard.
NOTE 2…
Soil quality — Gas chromatographic determination of the content of volatile aromatic hydrocarbons, n...
ISO 15009:2016 specifies a method for quantitative gas-chromatographic determination of volatile aromatic hydrocarbons, naphthalene and volatile halogenated hydrocarbons in soil.
This International Standard is applicable to all types of soil.
NOTE In the case of unsaturated peaty soils, absorption of the extraction solution may occur.
The lower limit of quantification is dependent on the…
IEC 60601-1:2005+A1:2012, 1.1 is replaced by:
ISO 11197:2016 applies to the basic safety and essential performance of medical supply units, hereafter also referred to as me equipment.
ISO 11197:2016 applies to medical supply units manufactured within a factory or assembled on site, including cabinetry and other enclosures, which incorporate patient care services.
NOTE 1 A party that…
Small bore connectors for liquids and gases in healthcare applications - Part 6: Connectors for neur...
ISO 80369-6:2016 specifies requirements for small-bore connectors intended to be used for connections in neuraxial applications. Neuraxial applications involve the use of medical devices intended to administer medications to neuraxial sites, wound infiltration anaesthesia delivery, and other regional anaesthesia procedures or to monitor or remove cerebro-spinal fluid for therapeutic or diagnostic…
Laveurs désinfecteurs — Partie 7: Exigences et essais pour les laveurs désinfecteurs destinés à la d...
ISO 15883-7:2016 spécifie les exigences particulières relatives aux laveurs désinfecteurs (LD) destinés à être utilisés pour le nettoyage et la désinfection chimique, au cours d'un seul cycle standard, d'articles réutilisables tels que les suivants:
a) les cadres de lit;
b) les tables de chevet;
c) les chariots de transport;
d) les récipients;
e) les tables d'…
STANDARD METHOD OF TESTS FOR DOOR CLOSERS INTENDED FOR USE WITH SWINGING DOORS
1.1 This Standard establishes requirements for door closers intended for use with swinging doors in fire
separations and on exit doors.
NOTE: Tests in this Standard are performed under laboratory conditions. In actual usage, results may vary because
of installation, maintenance and environmental conditions.
1.2 This Standard does not cover door closers equipped with hold-open features.
1.3…
Energy performance of large battery charger systems
1.1
This Standard specifies the test method for measuring and reporting the energy performance of large
battery charger systems.
Note: This Standard is technology neutral.
1.2
This Standard applies to large battery charger systems such as forklifts, autoettes, electric personal
assistive mobility devices, and low speed vehicles that are battery charger systems with a rated input
power of…
1.1
This Standard
a) specifies requirements for critical and semi-critical loaned, reusable medical devices; and
b) applies to all health care settings and vendors that use, send, receive, transport, or reprocess
loaned, reusable medical devices.
1.2
This Standard specifies requirements for
a) policies and standard operating procedures (SOPs) related to loaned, reusable medical devices;
b)…