GB 14232.3-2011
ActivePlastics collapsible containers for human blood and blood components － Part 3: Blood bag systems with integrated features
人体血液及血液成分袋式塑料容器 第3部分：含特殊组件的血袋系统
Application Summary AI generated
GB 14232.3-2011 specifies requirements for blood bag systems that include integrated features such as sampling devices, leukocyte reduction filters, or transfer tubing, focusing on safety, performance, and biocompatibility. It applies to the design, manufacturing, and testing of these specialized blood collection and storage systems used in healthcare settings, particularly in blood banks and transfusion services. The standard ensures that integrated components function reliably without compromising blood quality or patient safety during collection, processing, and transfusion.
Related Standards
GB/T 19381-2003
General methods of test for medical closures of butyl rubber
GB/T 14214-2003
Spectacle frames--General requirements and test methods
GB/T 18375.7-2004
Prosthetics--Structural testing of lower-limb prostheses--Part 7:Test submission document
GB/T 18375.6-2004
Prosthetics--Structural testing of lower-limb prostheses--Part 6:Loading parameters of supplementary structural tests
GB/T 18375.5-2004
Prosthetics--Structural testing of lower-limb prostheses--Part 5:Supplementary structural tests
GB/T 18375.8-2004
Prosthetics--Structural testing of lower-limb prostheses--Part 8:Test report
GB/T 19543-2004
Prostheses--Structural testing of hip units
GB/T 19629-2005
Medical Electrical Equipment-Dosimeters with ionization chambers and/or semi-conductors as used in X-ray diagnostic imaging
Transparency note: The application summary and key sentences on this page were automatically generated by AI from the standard's original text. This content has not been human-verified and should not be used for compliance or regulatory purposes. Always refer to the official standard document from the issuing authority.