GB/T 23101.3-2010
AbolishedImplants for surgery - Hydroxyapatite - Part 3: Chemical analysis and characterization of crystallinity and phase purity
外科植入物 羟基磷灰石 第3部分：结晶度和相纯度的化学分析和表征
Application Summary AI generated
This standard specifies chemical analysis methods and characterization criteria for crystallinity and phase purity of hydroxyapatite used in surgical implants. It is applied in the medical device industry for quality control and testing of hydroxyapatite coatings or bulk materials intended for bone repair, dental implants, and orthopedic prostheses. The standard ensures material consistency and biocompatibility by defining acceptable levels of secondary phases and crystalline structure.
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 19543-2004
Prostheses--Structural testing of hip units
GB/T 18375.8-2004
Prosthetics--Structural testing of lower-limb prostheses--Part 8:Test report
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.