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ISO 3826-4 - Plastics collapsible containers for human blood and blood components - Part 4: Aphaeresis blood bag systems with integrated features
August 1, 2015 - ISO

This part of ISO 3826 specifies requirements including performance requirements for aphaeresis blood bag systems with integrated features. Aphaeresis blood bag systems need not contain all of the integrated features identified in this part of ISO 3826. The integrated...

DIN EN ISO 3826-4 - Plastics collapsible containers for human blood and blood components - Part 4: Apheresis blood bag systems with integrated features (ISO 3826-4:2015)
December 1, 2015 - DIN

This part of ISO 3826 specifies requirements including performance requirements for aphaeresis blood bag systems with integrated features. Aphaeresis blood bag systems need not contain all of the integrated features identified in this part of ISO 3826. The integrated...

DS/EN ISO 3826-4 - Plastics collapsible containers for human blood and blood components - Part 4: Aphaeresis blood bag systems with integrated features (ISO 3826-4:2015)
September 15, 2015 - DS

This part of EN ISO 3826 specifies requirements, including performance requirements, for apheresis blood bag systems with integrated features. Apheresis blood bag systems need not contain all of the integrated features identified in this document. The integrated features...

DS/EN ISO 3826-3 - Plastics collapsible containers for human blood and blood components - Part 3: Blood bag systems with integrated features
January 14, 2008 - DS

This part of ISO 3826 specifies requirements, including performance requirements, for integrated features on plastics collapsible, non-vented, sterile containers (blood bag systems). Blood bag systems need not contain all of the integrated features identified in this...

ISO 3826-3 - Plastics collapsible containers for human blood and blood components Part 3: Blood bag systems with integrated features
September 15, 2006 - ISO

This part of ISO 3826 specifies requirements, including performance requirements, for integrated features on plastic, collapsible, non-vented, sterile containers (blood bag systems). Blood bag systems need not contain all of the integrated features identified in this...

MIL-S-36881 - STRIPPER, BLOOD BAG TUBING, ROLLER TYPE
NPFC
A description is not available for this item.
A-A-51963 - WEIGHT, BLOOD BAG, WATER BATH (LEAD)
NPFC
A description is not available for this item.
DS/EN ISO 8536-14 - Infusion equipment for medical use – Part 14: Clamps and flow regulators for transfusion and infusion equipment without fluid contact (ISO 8536-14:2016)
February 13, 2018 - DS

ISO 8536-14:2016 specifies requirements for non-sterile clamps and flow regulators used as a subcomponent to control the flow of intravenous solutions and/or blood components through sterilized infusion and blood transfusion sets and blood bag assemblies without fluid...

DIN EN ISO 8536-14 - Infusion equipment for medical use - Part 14: Clamps and flow regulators for transfusion and infusion equipment without fluid contact (ISO 8536-14:2016)
April 1, 2018 - DIN

This part of ISO 8536 specifies requirements for non-sterile clamps and flow regulators used as a subcomponent to control the flow of intravenous solutions and/or blood components through sterilized infusion and blood transfusion sets and blood bag assemblies without...

ASTM F2888 - Standard Practice for Platelet Leukocyte Count—An In-Vitro Measure for Hemocompatibility Assessment of Cardiovascular Materials
February 1, 2019 - ASTM

This practice assists in the evaluation of cardiovascular device materials for their ability to induce thrombus formation. Thrombus formation is assessed by means of a reduction in human platelets and leukocytes when consumed by thrombus after activation on the material surface. This assay may be...

A-A-53927 - INFUSOR, PRESSURE, BLOOD-INTRAVENOUS BAG
June 22, 1989 - NPFC

The General Services Administration has authorized the use of this commercial item description. This commerical item description covers expendable pressure infusors suitable for use with intravenous bags of 500 ml and 1000 ml capacity.

ASTM F2382 - Standard Test Method for Assessment of Circulating Blood-Contacting Medical Device Materials on Partial Thromboplastin Time (PTT)
October 1, 2018 - ASTM

This test method covers the screening of circulating blood-contacting device materials for their ability to induce blood coagulation via the intrinsic coagulation pathway. This assay should be part of the hemocompatibility evaluation for devices and materials contacting human...

ISO 8536-14 - Infusion equipment for medical use - Part 14: Clamps and flow regulators for transfusion and infusion equipment without fluid contact
November 15, 2016 - ISO

This part of ISO 8536 specifies requirements for non-sterile clamps and flow regulators used as a subcomponent to control the flow of intravenous solutions and/or blood components through sterilized infusion and blood transfusion sets and blood bag assemblies without...

A-A-53423 - BAG, BLOOD WARMING (DISPOSABLE)
NPFC
A description is not available for this item.
A-A-53973 - BAG, BLOOD COLLECTING-DISPENSING-SYSTEM
December 16, 1993 - NPFC

The General Services Administration has authorized the use of this Commercial Item Description. This Commercial Item Description covers sterile, pyrogen-free disposable, plastic, blood collecting component processing, and dispensing systems. Types I and II shall also provide blood...

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