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DS/EN ISO 15747 - PLASTIC CONTAINERS FOR INTRAVENOUS INJECTIONS (ISO 15747:2010) Organization: DS
Date: 2011-12-12
Description: ISO 15747:2010 contains requirements that relate to the safe handling and the physical, chemical and biological testing of plastic containers for parenterals. ISO 15747:2010 is applicable to plastic containers for parenterals having one or more chambers and having a total nominal capacity in the range of 50 ml to 5 000 ml such as film bags or blow-moulded plastic bottles for direct administration of infusion (injection) solutions.
NBN - EN ISO 15747 - PLASTIC CONTAINERS FOR INTRAVENOUS INJECTIONS (ISO 15747:2010) Organization: NBN
Date: 2011-12-14
Description: ISO 15747:2010 contains requirements that relate to the safe handling and the physical, chemical and biological testing of plastic containers for parenterals.ISO 15747:2010 is applicable to plastic containers for parenterals having one or more chambers and having a total nominal capacity in the range of 50 ml to 5 000 ml such as film bags or blow-moulded plastic bottles for direct administration of infusion (injection) solutions.
NBN - EN ISO 15747 - PLASTIC CONTAINERS FOR INTRAVENOUS INJECTIONS (ISO 15747:2010) Organization: NBN
Date: 2011-12-14
Description: ISO 15747:2010 contains requirements that relate to the safe handling and the physical, chemical and biological testing of plastic containers for parenterals.ISO 15747:2010 is applicable to plastic containers for parenterals having one or more chambers and having a total nominal capacity in the range of 50 ml to 5 000 ml such as film bags or blow-moulded plastic bottles for direct administration of infusion (injection) solutions.
DIN EN ISO 15747 - PLASTIC CONTAINERS FOR INTRAVENOUS INJECTIONS (ISO 15747:2010) Organization: DIN
Date: 2012-07-01
Description: This International Standard contains requirements that relate to the safe handling and the physical, chemical and biological testing of plastic containers for parenterals. This International Standard is applicable to plastic containers for parenterals having one or more chambers and having a total nominal capacity in the range of 50 ml to 5 000 ml such as film bags or blow-moulded plastic bottles for direct administration of infusion (injection) solutions.
AENOR - UNE-EN ISO 15747 - PLASTIC CONTAINERS FOR INTRAVENOUS INJECTIONS (ISO 15747:2010) Organization: AENOR
Date: 2012-02-22
SN - NS-EN ISO 15747:2011 - PLASTIC CONTAINERS FOR INTRAVENOUS INJECTIONS (ISO 15747:2010) Organization: SN
Date: 2012-01-01
SN - NS-EN ISO 15747:2010 - PLASTIC CONTAINERS FOR INTRAVENOUS INJECTIONS (ISO 15747:2010) Organization: SN
Date: 2010-07-01
NBN - EN ISO 3826-3 - PLASTICS COLLAPSIBLE CONTAINERS FOR HUMAN BLOOD AND BLOOD COMPONENTS - PART 3: BLOOD BAG SYSTEMS WITH INTEGRATED FEATURES (ISO 3826-3:2006) Organization: NBN
Date: 2008-03-20
Description: Unless otherwise specified, all tests specified in ISO 3826-3:2006 apply to the plastic container as prepared ready for use.
NBN - EN ISO 3826-3 - PLASTICS COLLAPSIBLE CONTAINERS FOR HUMAN BLOOD AND BLOOD COMPONENTS - PART 3: BLOOD BAG SYSTEMS WITH INTEGRATED FEATURES (ISO 3826-3:2006) Organization: NBN
Date: 2008-03-20
Description: Unless otherwise specified, all tests specified in ISO 3826-3:2006 apply to the plastic container as prepared ready for use.
ISO - ISO 3826-3 - PLASTICS COLLAPSIBLE CONTAINERS FOR HUMAN BLOOD AND BLOOD COMPONENTS PART 3: BLOOD BAG SYSTEMS WITH INTEGRATED FEATURES - FIRST EDITION Organization: ISO
Date: 2006-09-15
Description: Unless otherwise specified, all tests specified in this part of ISO 3826 apply to the plastic container as prepared ready for use. Use chemical, physical and biological tests in accordance with ISO 3826-1, where applicable.
DS/EN 868-5 - PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 5: SEALABLE POUCHES AND REELS OF POROUS MATERIALS AND PLASTIC FILM CONSTRUCTION - REQUIREMENTS AND TEST METHODS Organization: DS
Date: 2009-07-03
Description: NOTE 2 When additional materials are used inside the sterile barrier system in order to ease the organization, drying or aseptic presentation (e.g. inner wrap, container filter, indicators, packing lists, mats, instrument organizer sets, tray liners or an additional envelope around the medical device) then other requirements, including the determination of the acceptability of these materials during validation activities, may apply.
DIN EN 868-5 - PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 5: SEALABLE POUCHES AND REELS OF POROUS MATERIALS AND PLASTIC FILM CONSTRUCTION - REQUIREMENTS AND TEST METHODS Organization: DIN
Date: 2009-09-01
Description: NOTE 2 When additional materials are used inside the sterile barrier system in order to ease the organization, drying or aseptic presentation (e.g. inner wrap, container filter, indicators, packing lists, mats, instrument organizer sets, tray liners or an additional envelope around the medical device) then other requirements, including the determination of the acceptability of these materials during validation activities, may apply.
NBN - EN 868-5 - PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 5: SEALABLE POUCHES AND REELS OF POROUS MATERIALS AND PLASTIC FILM CONSTRUCTION - REQUIREMENTS AND TEST METHODS Organization: NBN
Date: 2009-07-17
Description: NOTE 2 When additional materials are used inside the sterile barrier system in order to ease the organization, dryingor aseptic presentation (e.g. inner wrap, container filter, indicators, packing lists, mats, instrument organizer sets, trayliners or an additional envelope around the medical device) then other requirements, including the determination of theacceptability of these materials during validation activities, may apply.
NBN - EN 868-5 - PACKAGING FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 5: SEALABLE POUCHES AND REELS OF POROUS MATERIALS AND PLASTIC FILM CONSTRUCTION - REQUIREMENTS AND TEST METHODS Organization: NBN
Date: 2009-07-17
Description: NOTE 2 When additional materials are used inside the sterile barrier system in order to ease the organization, dryingor aseptic presentation (e.g. inner wrap, container filter, indicators, packing lists, mats, instrument organizer sets, trayliners or an additional envelope around the medical device) then other requirements, including the determination of theacceptability of these materials during validation activities, may apply.
NBN - EN ISO 15747 - RÉCIPIENTS EN PLASTIQUE POUR INJECTIONS INTRAVEINEUSES (ISO 15747:2010) Organization: NBN
Date: 2011-12-14
Description: ISO 15747:2010 contains requirements that relate to the safe handling and the physical, chemical and biological testing of plastic containers for parenterals.ISO 15747:2010 is applicable to plastic containers for parenterals having one or more chambers and having a total nominal capacity in the range of 50 ml to 5 000 ml such as film bags or blow-moulded plastic bottles for direct administration of infusion (injection) solutions.
DIN EN ISO 175 - PLASTICS - METHODS OF TEST FOR THE DETERMINATION OF THE EFFECTS OF IMMERSION IN LIQUID CHEMICALS (ISO 175:2010) Organization: DIN
Date: 2011-03-01
Description: In this event, it is advisable to proceed exactly as indicated, but to suspend the specimen above the liquid, seal the container and maintain it at the test temperature throughout.
NBN - EN ISO 3826-3 - POCHES EN PLASTIQUE SOUPLE POUR LE SANG ET LES COMPOSANTS DU SANG - PARTIE 3: SYSTÈMES DE POCHES POUR LE SANG AVEC ACCESSOIRES INTÉGRÉS (ISO 3826-3:2006) Organization: NBN
Date: 2008-03-20
Description: Unless otherwise specified, all tests specified in ISO 3826-3:2006 apply to the plastic container as prepared ready for use.
DSF/PREN 16436 - RUBBER AND PLASTIC HOSES AND TUBINGS FOR USE WITH PROPANE, BUTANE AND THEIR MIXTURES IN THE VAPOUR PHASE Organization: DS
Description: This European Standard specifies the characteristics and performance requirements for tubing and hoses made of either rubber or plastics for use with commercial propane and butane and mixtures thereof, in the vapour phase, for the connection of appliances (i.e. for instance, from pressurized gas container to a regulator, or a regulator to an appliance or to a metal tube, or an appliance to a valve) in environments in a temperature range from -30 °C to +70 °C.
BSI - PREN 16436 - RUBBER AND PLASTIC HOSES AND TUBINGS FOR USE WITH PROPANE, BUTANE AND THEIR MIXTURES IN THE VAPOUR PHASE Organization: BSI
Date: 2012-05-01
Description: This European Standard specifies the characteristics and performance requirements for tubing and hoses made of either rubber or plastics for use with commercial propane and butane and mixtures thereof, in the vapour phase, for the connection of appliances (i.e. for instance, from pressurized gas container to a regulator, or a regulator to an appliance or to a metal tube, or an appliance to a valve) in environments in a temperature range from –30 °C to +70 °C.
DIN EN ISO 24234 - DENTISTRY - DENTAL AMALGAM (ISO 24234:2015) Organization: DIN
Date: 2015-08-01
Description: This International Standard is not applicable to mercury supplied in masses greater than this in a single primary container (i.e. dental mercury in bulk). Dental mercury supplied in bulk volumes will not conform to this International Standard.

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