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1.1 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 part of the hemocompatibility evaluation for devices and materials contacting human blood, as in accordance with ANSI/AAMI/ISO 10993–4. See also Test Method F2382.
Author | ASTM |
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Editor | ASTM |
Document type | Standard |
Format | File |
ICS | 11.100.30 : Analysis of blood and urine |
Number of pages | 5 |
Replace | ASTM F2888-13 + Redline |
Year | 2019 |
Document history | ASTM F2888-13 + Redline |
Country | USA |
Keyword | ASTM 2888;ASTM F2888;ASTM F2888;10.1520/F2888-19 |